The following data is part of a premarket notification filed by Microsurge, Inc. with the FDA for Microsurge Front-end Grasping Devices.
| Device ID | K922802 |
| 510k Number | K922802 |
| Device Name: | MICROSURGE FRONT-END GRASPING DEVICES |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | MICROSURGE, INC. 45 WEST ST. SUITE 2 Attleboro, MA 02703 |
| Contact | James R Veale |
| Correspondent | James R Veale MICROSURGE, INC. 45 WEST ST. SUITE 2 Attleboro, MA 02703 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-06-10 |
| Decision Date | 1993-01-29 |