Who else makes this device?

Name: Stretcher Scale Upgrade KIT W/J-Hooks, Wide (Models With O2 Tank)
Brand: Stretcher Scale Upgrade KIT W/J-Hooks, Wide (Models With O2 Tank)

General Hospital › MiscellaneousStretcher, Wheeled

Stretcher Scale Upgrade KIT W/J-Hooks, Wide (Models With O2 Tank)

Catalogue number P746A04, listed by Hill-ROM, Inc., United States, under Stretcher, Wheeled. 31 manufacturers in China are registered for this product code.

Registry build 21.09.26

31manufacturers in China registered for this device type

1catalogue number

4510(k) clearances naming this product code

1recall

Who Else Makes It

Concentrated in Jiangsu (15), Hebei (7), Guangdong (6). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FPO
Manufacturer	City	Province	Registered as	Device types
Hengshui Gangsheng Medical Instruments Co., Ltd.	Hengshui	Hebei	Contract manufacturer	36
Zhangjiagang Xiehe Medical Apparatus & Instruments Co., Ltd.	Zhangjiagang	Jiangsu	Contract manufacturer	11
Hospital & Homecare IMP. & EXP. Co., Ltd.	Nanjing	Jiangsu	Contract manufacturer	179
Danyang NEW Hope Medical Equipment Co., Ltd.	Danyang	Jiangsu	Manufacturer	38
Jiangsu Saikang Medical Equipment Co., Ltd.	Zhangjiagang	Jiangsu	Contract manufacturer	34
Jiangsu Yongfa Medical Equipment Technology Co., Ltd.	Zhangjiagang	Jiangsu	Manufacturer	33
Shanghai NO. 2 Medical College Duhang Medical Equipment Factory	Shanghai	Shanghai	Contract manufacturer	32
Jiangsu Rooe Medical Technology Co., Ltd.	Zhangjiagang	Jiangsu	Manufacturer	31
Better Medical Technology Co., Ltd.	Foshan	Guangdong	Manufacturer	24
Shenyang Ourpromise Medical Equipment Co., Ltd.	Shenyang	Liaoning	Manufacturer	24
Foshan Fuzikon Medical Technology Co., Ltd.	Foshan	Guangdong	Manufacturer	21
Jiangsu Sintang Health&Technology Co., Ltd.	Yancheng	Jiangsu	Manufacturer	21

Showing 12 of 31. All 31 manufacturers in China registered for Stretcher, Wheeled

Record

Regulatory record for Stretcher Scale Upgrade KIT W/J-Hooks, Wide (Models With O2 Tank)
Listed by	Hill-ROM, Inc., United States
FDA product code	FPO
Device type	Stretcher, Wheeled
Device class	Class 2
Regulation	21 CFR 880.6910
Establishment	Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Premarket notification	Exempt
Record published	2020-07-14
Record revised	2022-06-22 (version 2)

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Label carries	lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Stretcher Scale Upgrade KIT W/J-Hooks, Wide (Models With O2 Tank)
Catalogue number	Size	Status
P746A04		In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
Sechrist Industries, Inc.	Sechrist Industries, Inc.	51
Stretcher, Wheeled	Gendron, Inc.	40
Stretcher, Wheeled	Stryker GmbH	35
Havasu	Stryker GmbH	29
MJM 900 Series Gurney	M J M International Corporation	27
Sprint 100	L I N E T spol. s r.o.	27
Hausted	GF Health Products, Inc	24
Mondial® Monobloc	Ferno-Washington, Inc.	24
Mondial® Transporter	Ferno-Washington, Inc.	20
Prime Series	Stryker GmbH	18
Pedigo Products, Inc.	Pedigo Products, Inc.	15
Zephyr Patient Stretcher	Diacor, Inc.	14

Showing 12 of 182. All products under Stretcher, Wheeled

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance	Decision date
K961437	1996-06-03
K952447	1995-11-22
K922809	1993-03-31
K922808	1993-03-31

Recalls

The FDA has not published a severity grade for these. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated	FDA class	Root cause	Reason	Quantity	Closed
2008-04-03	Not classified	Device Design	The auto contour function on/off handle may be inadvertently activated while the head of the stretcher is raised, increasing the possibility of the head section to become jammed and preventing it from lowering. This may result in a delay t	564	2009-12-29

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.