# Pro-Lab, Inc.

- Location (FDA's records): Ontario Canada M5m 1c9, CA
- FDA decisions: 27 (1984–1995): 27 510(k) clearances
- Product codes: JSK (7), JTO (3), JSE (2), FRG (2), LHL (1), HIO (1), JTR (1), GNA (1), GTZ (1), JSX (1), LRP (1), FSM (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Clinical Innovations, Inc.: 1 (https://510kreport.com/company/clinical-innovations)
- Common Sense, Ltd.: 1 (https://510kreport.com/company/common-sense)

## Its most-cited devices
- K914419: Amniotest (TM) (1993), cited by 2

## Recent decisions
- K934383: Prolex (Streptoccal Grouping Latex Kit) (Jan 27, 1995)
- K914419: Amniotest (TM) (Sep 1, 1993)
- K921421: Legionella Reagens for Direct Fluorescent Antibody (Jul 28, 1992)
- K903714: E. Coli 0157 Latex Test (Jan 24, 1991)
- K894221: Rosco Pyrr (Sep 28, 1989)
- K883995: X-Act Urea/Tda (Oct 12, 1988)
- K883996: X-Act LDC/Ind (Oct 12, 1988)
- K871121: Protect T.M. (Apr 14, 1987)

Source page: https://510kreport.com/company/pro-lab