# Hancock Laboratories, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 5 (1978–1980): 5 510(k) clearances
- Product codes: DTI (1), DWS (1), DQO (1), KRH (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Cardio Medical Solutions, Inc.: 1 (https://510kreport.com/company/cardio-medical-solutions)

## Its most-cited devices
- K800122: Hancock Aortic Punch (1980), cited by 1

## Recent decisions
- K801885: Hancock * Obturators (Sep 9, 1980)
- K800703: Modified Catheter Package (Apr 8, 1980)
- K800122: Hancock Aortic Punch (Feb 1, 1980)
- K790534: Mersilene Sutures (Mar 26, 1979)
- K780568: Duran Flexible Ring (May 26, 1978)

Source page: https://510kreport.com/company/hancock-laboratories