# K921968: IN Vitro Diagnostic Reagent Set, Indir. Preg. Test

- Pathway: 510(k) (Traditional)
- Applicant: Tech-Co, Inc.
- Decided: Jun 28, 1996 after 1,523 days
- Product code: JHJ (Agglutination Method, Human Chorionic Gonadotropin)
- Device class: 2
- Regulation: 21 CFR 862.1155
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

Source page: https://510kreport.com/device/K921968
Methodology: https://510kreport.com/methodology