The following data is part of a premarket notification filed by Dexide, Inc. with the FDA for Multachoice Instruments.
| Device ID | K991814 |
| 510k Number | K991814 |
| Device Name: | MULTACHOICE INSTRUMENTS |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | DEXIDE, INC. 7509 FLAGSTONE DR. Fort Worth, TX 76118 -6995 |
| Contact | John Corzine |
| Correspondent | John Corzine DEXIDE, INC. 7509 FLAGSTONE DR. Fort Worth, TX 76118 -6995 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-05-27 |
| Decision Date | 1999-06-23 |
| Summary: | summary |