The following data is part of a premarket notification filed by Honeywell, Inc. with the FDA for Telemetry Transmitter & Receiver.
| Device ID | K813064 |
| 510k Number | K813064 |
| Device Name: | TELEMETRY TRANSMITTER & RECEIVER |
| Classification | Transmitters And Receivers, Physiological Signal, Radiofrequency |
| Applicant | HONEYWELL, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | DRG |
| CFR Regulation Number | 870.2910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-10-30 |
| Decision Date | 1981-12-29 |