Test Kits

Oxidase Swabs

Registry build 21.09.26
4manufacturers in China registered for this device type
2catalogue numbers in this listing
7510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Jiangsu (1), Shandong (1), Jilin (1).

Chinese manufacturers registered for FDA product code JTO
Manufacturer City Province Registered as Device types
Hospital & Homecare IMP. & EXP. Co., Ltd. Nanjing Jiangsu Contract manufacturer 179
Jinan Babio Biotechnology Co., Ltd. Jinan Shandong Manufacturer 25
Changchun LYZ Technology Co., Ltd. Changchun Jilin Manufacturer 16
Zhejiang Joozena Medical Technology Co., Ltd. Dongyang City, Jinhua Zhejiang Manufacturer 5

Record

Regulatory record for Test Kits
Listed by Microbiologics, Inc., United States
FDA product code JTO
Device type Discs, Strips And Reagents, Microorganism Differentiation
Device class Class 1
Regulation 21 CFR 866.2660
Establishment Contract manufacturer, Repacker / relabeller, Manufacturer
Premarket notification Exempt
Record published 2022-09-26
Record revised 2022-11-28 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 8 °C

Catalogue Numbers

Catalogue numbers for Test Kits
Catalogue number Size Status
60060 In distribution
60500 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Remel Remel, Inc. 62
Discs, Strips And Reagents, Microorganism Differentiation Hardy Diagnostics 37
HardyDisk™ Hardy Diagnostics 17
Bactidrop Remel, Inc. 10
Redipor Analytichem USA, Inc. 7
BD BBL™ Taxo™ P Becton, Dickinson AND Company 4
BD BBL™ Taxo™ A Becton, Dickinson AND Company 4
API® NaCl 0.85% Medium bioMerieux, Inc. 3
Bacticard Remel, Inc. 3
Chemmette Reagents Microbiologics, Inc. 2
Optochin Oxoid, Ltd. 2
X Factor Oxoid, Ltd. 2

Showing 12 of 139. All products under Discs, Strips And Reagents, Microorganism Differentiation

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K970009 1997-02-06
K954812 1995-12-20
K951889 1995-08-24
K945883 1995-04-24
K945881 1995-04-24
K945882 1995-04-24
K945880 1995-04-24

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
2021-07-01 Class II Mixed-up of materials/components A lot of KOH 10% was made with Hydrogen Peroxide 3% instead of KOH 10%. 11 kits 2023-05-02

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