SLT Ivus P1 Cart

Catalogue number CART01, listed by Provisio Medical Inc., United States, under Catheter, Ultrasound, Intravascular. 4 manufacturers in China are registered for this product code.

Registry build 21.09.26
4manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (3), Shanghai (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code OBJ
Manufacturer City Province Registered as Device types
Philips Ultrasound (Shanghai) Co., Ltd. Shanghai Shanghai Contract manufacturer 5
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57
Jiangsu Tingsn Technology Co., Ltd. Nanjing Jiangsu Manufacturer 4
Nanjing Shuangwei Biotechnology Co., Ltd. Nanjing Jiangsu Contract manufacturer 1

Record

Regulatory record for SLT Ivus P1 Cart
Listed by Provisio Medical Inc., United States
FDA product code OBJ
Device type Catheter, Ultrasound, Intravascular
Device class Class 2
Regulation 21 CFR 870.1200
Establishment Manufacturer
510(k) K233948
Record published 2024-05-24

Specifications

Specifications
MRI safety MR Unsafe
Prescription Prescription only
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for SLT Ivus P1 Cart
Catalogue number Size Status
CART01 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Arrow Teleflex Medical LLC 27
Acist HDi® HD Ivus System Acist Medical Systems, Inc. 8
Soundstar Biosense Webster, Inc. 6
OptiCross Boston Scientific Corporation 4
Busse Hospital Disposables Robert Busse & Co., Inc. 4
Acist HDi® System Console Acist Medical Systems, Inc. 4
OptiCross™ 6 Boston Scientific Corporation 3
7 Fr PV-Catheter CD Leycom 3
NES Reprocessed Visions PV.014P RX Digital Ivus Catheter North East Scientific Inc 3
OptiCross™ 6 HD Boston Scientific Corporation 2
Acist HDi® Bed Rail Mount Acist Medical Systems, Inc. 2
4 Fr PV Catheter CD Leycom 2

Showing 12 of 63. All products under Catheter, Ultrasound, Intravascular

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K233948 2024-04-23

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.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer