# Flexsite Diagnostics, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 2 (1997–2000): 2 510(k) clearances
- Product codes: LCP (1), JIR (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 6 (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 whose devices it cites most
- Awareness Technology, Inc.: 1 (https://510kreport.com/company/awareness-technology)

## Firms that cite its devices most
- Biosafe Laboratories, Inc.: 1 (https://510kreport.com/company/biosafe-laboratories)
- Medisense, Inc.: 1 (https://510kreport.com/company/medisense)
- Diabetes Technologies, Inc. (Dti): 1 (https://510kreport.com/company/diabetes-technologies-dti)
- Osborn Laboratories, Inc.: 1 (https://510kreport.com/company/osborn-laboratories)
- Osborn Group, Inc.: 1 (https://510kreport.com/company/osborn-group)
- Boehringer Mannheim Corp.: 1 (https://510kreport.com/company/boehringer-mannheim)

## Its most-cited devices
- K971919: Ezchek/Hba Blood Collection Kit (1997), cited by 6

## Recent decisions
- K001810: Urisite Urine Collection Kit for Microalbumin/Creatinine Testing (Aug 14, 2000)
- K971919: Ezchek/Hba Blood Collection Kit (Sep 5, 1997)

Source page: https://510kreport.com/company/flexsite-diagnostics