The following data is part of a premarket notification filed by Gaymar Industries, Inc. with the FDA for Weighing Station, Mobile Patient.
| Device ID | K760545 |
| 510k Number | K760545 |
| Device Name: | WEIGHING STATION, MOBILE PATIENT |
| Classification | Scale, Patient |
| Applicant | GAYMAR INDUSTRIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FRW |
| CFR Regulation Number | 880.2720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-08-30 |
| Decision Date | 1976-11-12 |