The following data is part of a premarket notification filed by Medical Specialties, Inc. with the FDA for Kwik-awa Vest.
| Device ID | K791363 |
| 510k Number | K791363 |
| Device Name: | KWIK-AWA VEST |
| Classification | Transmitters And Receivers, Physiological Signal, Radiofrequency |
| Applicant | MEDICAL SPECIALTIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DRG |
| CFR Regulation Number | 870.2910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-07-17 |
| Decision Date | 1979-08-03 |