# Cameron-Miller, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 14 (1977–1994): 14 510(k) clearances
- Product codes: GEI (10), HGI (2), KNS (1), FCT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K944775: Electrosurgical Unit Model 26-0335 (Oct 11, 1994)
- K931541: Model 26-0375, Electrosurgical Generator (Jun 1, 1994)
- K931437: Model 80-1983, Electrosurgical Generator (May 27, 1994)
- K935490: Electrosurgical Device, Model 26-2500 (Apr 1, 1994)
- K854109: Electrosurgical Devices, 26-0330,26-335,340 & 0345 (Jan 24, 1986)
- K853972: Cameron-Miller Model 80-2701, Bipolar Coagulator (Jan 24, 1986)
- K833449: Hand Controlled Pencil or Switch Hand (Nov 29, 1983)
- K822092: Cameron-Miller #40-1516 (Sep 21, 1982)

Source page: https://510kreport.com/company/cameron-miller