The following data is part of a premarket notification filed by Btl Industries Inc. with the FDA for Btl-899 Fp.
| Device ID | K211107 |
| 510k Number | K211107 |
| Device Name: | BTL-899 FP |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | BTL Industries Inc. 362 Elm Street Marlborough, MA 01752 |
| Contact | David Chmel |
| Correspondent | David Chmel BTL Industries Inc. 362 Elm Street Marlborough, MA 01752 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-04-14 |
| Decision Date | 2021-07-09 |