The following data is part of a premarket notification filed by Aesculap, Inc. with the FDA for Caiman Seal And Cut Technology.
| Device ID | K140839 |
| 510k Number | K140839 |
| Device Name: | CAIMAN SEAL AND CUT TECHNOLOGY |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | AESCULAP, INC. 3773 Corporate Parkway Center Valley, PA 18034 |
| Contact | Denise Adams |
| Correspondent | Denise Adams AESCULAP, INC. 3773 Corporate Parkway Center Valley, PA 18034 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-04-02 |
| Decision Date | 2014-04-28 |
| Summary: | summary |