# Stephen Chakoff, Inc.

- Location (FDA's records): Miami, FL
- FDA decisions: 16 (1993–1995): 16 510(k) clearances
- Product codes: GCJ (10), FDG (1), FCW (1), FWF (1), EOB (1), GEI (1), HIH (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
- K940316: Hysterscope (Nov 16, 1995)
- K940317: Sinuscope (May 24, 1995)
- K950753: Chakoff Endoscopy (Camera Television Endoscopic Without Audio (May 15, 1995)
- K951082: Chakoff Endoscopy, Rigid Endoscope (Mar 22, 1995)
- K950747: Chakoff Endoscopy (Light Source Endoscopic Xenon Arc.) (Mar 6, 1995)
- K950748: Chakoff Endoscopy (Fiber Optic Light Source Routine) (Mar 6, 1995)
- K950745: Chakoff Endoscopy (Endoscope and/or Accessories) (Mar 6, 1995)
- K950746: Chakoff Endoscopy (Set Laparoscopy) (Mar 6, 1995)

Source page: https://510kreport.com/company/stephen-chakoff