MODULAP
Electrosurgical, Cutting & Coagulation & Accessories
ATC TECHNOLOGIES, INC.
The following data is part of a premarket notification filed by Atc Technologies, Inc. with the FDA for Modulap.
Pre-market Notification Details
| Device ID | K994319 |
| 510k Number | K994319 |
| Device Name: | MODULAP |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | ATC TECHNOLOGIES, INC. 1034 LINCOLN ST. Hollywood, FL 33019 |
| Contact | Marian Harding Cochran |
| Correspondent | Marian Harding Cochran ATC TECHNOLOGIES, INC. 1034 LINCOLN ST. Hollywood, FL 33019 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-12-22 |
| Decision Date | 2000-03-20 |
| Summary: | summary |
Trademark Results [MODULAP]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MODULAP 75494836 2264815 Live/Registered |
ATC Technologies, Inc. 1998-06-02 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.