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 |