# Medical Products Development, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 13 (1980–1981): 13 510(k) clearances
- Product codes: HQP (4), GEI (3), FSQ (3), HAM (2), HQO (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
- Bovie Medical Corporation: 1 (https://510kreport.com/company/bovie-medical)

## Its most-cited devices
- K810017: Microsurg Cautery (1981), cited by 1

## Recent decisions
- K810016: Replacable Battery Perfectemp Cautery (Apr 23, 1981)
- K810012: Multimicro Surgical Cautery (Apr 23, 1981)
- K810013: Multiperfectemp Cautery (Apr 23, 1981)
- K803067: Surg-Flex 10 Light (Feb 26, 1981)
- K810014: Replacable Battery HI-Temp Cautery (Feb 12, 1981)
- K810015: Multihi-Temp Cautery (Feb 12, 1981)
- K802942: Hitemp. TM 2 Looptip Cautery (Feb 4, 1981)
- K810019: Surg-Flex 15 Surgical Light (Jan 23, 1981)

Source page: https://510kreport.com/company/medical-products-development