The following data is part of a premarket notification filed by Circon Video with the FDA for Circon Acmi Gen Surg Instru For Mini Invasive Surg.
| Device ID | K914883 |
| 510k Number | K914883 |
| Device Name: | CIRCON ACMI GEN SURG INSTRU FOR MINI INVASIVE SURG |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | CIRCON VIDEO 300 STILLWATER AVE. P.O. BOX BOX 1971 Stanford, CT 06904 -1971 |
| Contact | Ervin F Taylor |
| Correspondent | Ervin F Taylor CIRCON VIDEO 300 STILLWATER AVE. P.O. BOX BOX 1971 Stanford, CT 06904 -1971 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-10-30 |
| Decision Date | 1993-01-15 |