# K260342: AllTest Strep A Rapid Test

- Pathway: 510(k) (Traditional)
- Applicant: Hangzhou AllTest Biotech Co., Ltd.
- Decided: Apr 30, 2026 after 87 days
- Product code: GTY (Antigens, All Groups, Streptococcus Spp.)
- Device class: 1
- Regulation: 21 CFR 866.3740
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K971349 (1997). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133343: Wondfo Rapid Strep a Test, Guangzhou Wondfo Biotech Co., Ltd. (2014) Summary page 5.

## Indications for use
The AllTest Strep A Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of Streptococcus pyogenes (Group A β-hemolytic Streptococcus, Strep A) antigens in throat swab specimens from patients with signs and symptoms of pharyngitis to aid in the diagnosis of Group A Streptococcus infection. All negative test results should be confirmed by bacterial culture because negative results do not preclude infection with Group A Streptococcus and should not be used as the sole basis for treatment.

Source page: https://510kreport.com/device/K260342
Methodology: https://510kreport.com/methodology