The following data is part of a premarket notification filed by Megadyne Medical Products, Inc. with the FDA for Tbd.
| Device ID | K972273 |
| 510k Number | K972273 |
| Device Name: | TBD |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | MEGADYNE MEDICAL PRODUCTS, INC. 11506 SOUTH STATE ST. Draper, UT 84020 |
| Contact | John W Smith |
| Correspondent | John W Smith MEGADYNE MEDICAL PRODUCTS, INC. 11506 SOUTH STATE ST. Draper, UT 84020 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-06-18 |
| Decision Date | 1997-07-08 |
| Summary: | summary |