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FDA 510(k)

WEIGHING STATION, MOBILE PATIENT

K-Number: K760545 · 1976-11-12

ApplicantGaymar Industries, Inc.
Decision Date1976-11-12
Product CodeFRW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WEIGHING STATION, MOBILE PATIENT is the device name listed in this FDA 510(k) record. The listed applicant is Gaymar Industries, Inc.. It received FDA 510(k) clearance on 1976-11-12 under 510(k) number K760545. The device is classified under product code FRW. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WEIGHING STATION, MOBILE PATIENT?

WEIGHING STATION, MOBILE PATIENT is a medical device that received FDA 510(k) clearance on 1976-11-12. The listed applicant is Gaymar Industries, Inc.. The 510(k) number is K760545.

When did WEIGHING STATION, MOBILE PATIENT receive FDA 510(k) clearance?

WEIGHING STATION, MOBILE PATIENT received FDA 510(k) clearance on 1976-11-12, under 510(k) number K760545.

Who is the listed applicant for WEIGHING STATION, MOBILE PATIENT?

The FDA 510(k) record lists Gaymar Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WEIGHING STATION, MOBILE PATIENT?

The FDA product code for WEIGHING STATION, MOBILE PATIENT is FRW.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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