# Clinical Technology Corp.

- Location (FDA's records): Rochester, NY
- FDA decisions: 12 (1982–1994): 12 510(k) clearances
- Product codes: GEI (3), FRC (1), LXH (1), GHM (1), FLL (1), LFL (1), EFB (1), LBK (1), LCP (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Getinge USA, Inc.: 1 (https://510kreport.com/company/getinge-usa)
- Satelec: 1 (https://510kreport.com/company/satelec)

## Its most-cited devices
- K872867: Biosign (1988), cited by 1
- K855138: Bovie Ultrasonic Surgical System (1986), cited by 1

## Recent decisions
- K925080: Tek-Lube (Jan 31, 1994)
- K872867: Biosign (Jul 6, 1988)
- K880166: Bovie Ultrasonic Surgical Aspirator, Model ME2000 (Feb 18, 1988)
- K872705: Bovie 400-CT Electrosurgical Generator (Unit) (Sep 1, 1987)
- K855138: Bovie Ultrasonic Surgical System (Nov 10, 1986)
- K854231: Electrosurgical Cutting & Coagulation Device/Acces (May 2, 1986)
- K853507: Steri-Grip (Sep 5, 1985)
- K852986: Glyco-Sep/Alc Test Kit for Separat of Hemoglobin (Aug 19, 1985)

Source page: https://510kreport.com/company/clinical-technology