AdTec
Laparoscope, General & Plastic Surgery
AESCULAP, INC.
The following data is part of a premarket notification filed by Aesculap, Inc. with the FDA for Adtec.
Pre-market Notification Details
| Device ID | K160393 |
| 510k Number | K160393 |
| Device Name: | AdTec |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | AESCULAP, INC. 3773 CORPORATE PARKWAY Center Valley, PA 18034 |
| Contact | Jessica Stigliano |
| Correspondent | Jessica Stigliano AESCULAP, INC. 3773 CORPORATE PARKWAY Center Valley, PA 18034 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-02-11 |
| Decision Date | 2016-05-26 |
| Summary: | summary |
Trademark Results [AdTec]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ADTEC 73361148 1277837 Dead/Cancelled |
Ad-Tec Products, Inc. 1982-04-23 |
 ADTEC 73037685 1041742 Live/Registered |
AD-TEC PRODUCTS, INC. 1974-11-20 |
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