Hemoccult

Hemoccult ICT Immunochemical Fecal Occult Blood Test Controls

Registry build 21.09.26
5manufacturers in China registered for this device type
17catalogue numbers in this listing
1510(k) clearance
1recall

Who Else Makes It

Concentrated in Zhejiang (2), Guangdong (1), Beijing (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KHE
Manufacturer City Province Registered as Device types
Zhejiang Orient Gene Biotech Huzhou Zhejiang Contract manufacturer 86
Hangzhou Genesis Biodetection & Biocontrol Co., Ltd. Hangzhou Zhejiang Contract manufacturer 5
Guangzhou Wondfo Biotech Co., Ltd. Guangzhou Guangdong Contract manufacturer 44
W.h.p.m. Bioresearch & Technology Co., Ltd. Beijing Beijing Manufacturer 37
Chong Qing Teco Huayi Pharm. Co. Shapingba Dist. Chongqing Contract manufacturer 18

Record

Regulatory record for Hemoccult
Listed by Beckman Coulter, Inc., United States
FDA product code KHE
Device type Reagent, Occult Blood
Device class Class 2
Regulation 21 CFR 864.6550
Establishment Contract manufacturer, Specification developer, Manufacturer, Exporter
Premarket notification Exempt
Record published 2016-09-23
Record revised 2023-06-19 (version 6)

Specifications

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

Catalogue Numbers

Catalogue numbers for Hemoccult
Catalogue number Size Status
64130 In distribution
395068 In distribution
A96636 In distribution
61200 In distribution
60152 In distribution
395261 In distribution
395065 In distribution
64152 In distribution
60151 In distribution
395066 In distribution
64151 In distribution
63202 In distribution
61100 In distribution
62115 In distribution
61130 In distribution
395067 In distribution
64115 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
OC-Light S Polymedco Cancer Diagnostic Products LLC 59
McKesson Mckesson Medical-Surgical Inc. 21
Hemosure Hemosure Inc. 21
Henry Schein Henry Schein, Inc. 14
PremierPro Prestige Ameritech 11
hema-screen Specific Immunostics, Inc. 9
InSure® ONE™ Enterix Inc. 8
InSure FIT Enterix Inc. 7
hema-screen Immunostics, Inc. 7
ADS Medical W.h.p.m., Inc. 7
QuickVue Quidel Corp. 6
Medline Medline Industries, Inc. 5

Showing 12 of 135. All products under Reagent, Occult Blood

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K080812 2008-06-25

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. 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
2013-07-17 Class II Under Investigation by firm Beckman Coulter has received a customer complaint that suggests trending of
positive results has increased from approximately 4% to 1 0%. As a result of our
investigation, Beckman Coulter has confirmed an increase in sensitivity at the
bord
68,116 units 2014-10-24

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