The following data is part of a premarket notification filed by Dornier Surgical Products, Inc. with the FDA for Dornier Medilas E.
| Device ID | K981438 |
| 510k Number | K981438 |
| Device Name: | DORNIER MEDILAS E |
| Classification | Powered Laser Surgical Instrument |
| Applicant | DORNIER SURGICAL PRODUCTS, INC. 1155 ROBERTS BLVD. Kennesaw, GA 30144 |
| Contact | Carol Werencke |
| Correspondent | Carol Werencke DORNIER SURGICAL PRODUCTS, INC. 1155 ROBERTS BLVD. Kennesaw, GA 30144 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-04-21 |
| Decision Date | 1998-07-20 |
| Summary: | summary |