The following data is part of a premarket notification filed by Medar Corp., Inc. with the FDA for Medar Apm Force Transducer.
| Device ID | K853849 |
| 510k Number | K853849 |
| Device Name: | MEDAR APM FORCE TRANSDUCER |
| Classification | Stimulator, Nerve, Battery-powered |
| Applicant | MEDAR CORP., INC. P.O. BOX N-H Scarsdale, NY 10583 |
| Contact | George Stanec |
| Correspondent | George Stanec MEDAR CORP., INC. P.O. BOX N-H Scarsdale, NY 10583 |
| Product Code | BXN |
| CFR Regulation Number | 868.2775 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-09-16 |
| Decision Date | 1986-01-03 |