# American Micro Scan

- Location (FDA's records): West Sacramento, CA
- FDA decisions: 25 (1979–1987): 24 510(k) clearances and 1 original PMA approval
- Product codes: JWY (3), LJP (2), JTO (2), JTA (1), GRP (1), LQL (1), JJQ (1), JSM (1), JWX (1), GWC (1), LDW (1), JTS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Diagnostic Hybrids, Inc.: 1 (https://510kreport.com/company/diagnostic-hybrids)

## Its most-cited devices
- K864389: Chlamydiae Flourescent Monoclonal Antibody Test (1986), cited by 1

## Recent decisions
- K870029: Immunoscan (TM) Direct Streptococcus Pneumoniae (Mar 25, 1987)
- K864662: Chlamydiae Fluor. AB Test for Detection in Smears (Mar 25, 1987)
- K863776: Microdilution Mic Panels (Feb 2, 1987)
- K864674: Microdilution Identification Panels (Jan 5, 1987)
- K864389: Chlamydiae Flourescent Monoclonal Antibody Test (Dec 4, 1986)
- K863038: Gram Positive Fluorescent Identification Panel (Sep 30, 1986)
- K862642: Gram Negative Fluorescent Identification Panel (Sep 11, 1986)
- K862332: Anaerobe Rapid Chromogenic ID Panel (Aug 27, 1986)

Source page: https://510kreport.com/company/american-micro-scan