# Osborn Group, Inc.

- Location (FDA's records): Olathe, KS
- FDA decisions: 4 (1999–2000): 4 510(k) clearances
- Product codes: CGX (1), JKA (1), LCP (1), JIQ (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 37 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Osborn Laboratories, Inc.: 2 (https://510kreport.com/company/osborn-laboratories)
- Diabetes Technologies, Inc. (Dti): 1 (https://510kreport.com/company/diabetes-technologies-dti)
- Flexsite Diagnostics, Inc.: 1 (https://510kreport.com/company/flexsite-diagnostics)
- Sage Products, Inc.: 1 (https://510kreport.com/company/sage-products)

## Firms that cite its devices most
- Home Access Health Corp.: 1 (https://510kreport.com/company/home-access-health)
- Immunetech Corporation: 1 (https://510kreport.com/company/immunetech)

## Its most-cited devices
- K993787: Appraise-Cardio Sample Collection Kit (2000), cited by 1
- K990899: Hemochek-A1C Sample Collection Kit (1999), cited by 1

## Recent decisions
- K002156: Appraise Urine Microalbumin Collection Kit (Dec 19, 2000)
- K993787: Appraise-Cardio Sample Collection Kit (Apr 14, 2000)
- K990899: Hemochek-A1C Sample Collection Kit (Dec 21, 1999)
- K991800: Hemochek Urine Collection Kit (Sep 24, 1999)

Source page: https://510kreport.com/company/osborn-group