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FDA 510(k)

PATIENT TURNING AND REPOSITIONING G DEV.

K-Number: K770499 · 1977-04-29

ApplicantPatient Healthguards Corp.
Decision Date1977-04-29
Product CodeFMR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT TURNING AND REPOSITIONING G DEV. is the device name listed in this FDA 510(k) record. The listed applicant is Patient Healthguards Corp.. It received FDA 510(k) clearance on 1977-04-29 under 510(k) number K770499. The device is classified under product code FMR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT TURNING AND REPOSITIONING G DEV.?

PATIENT TURNING AND REPOSITIONING G DEV. is a medical device that received FDA 510(k) clearance on 1977-04-29. The listed applicant is Patient Healthguards Corp.. The 510(k) number is K770499.

When did PATIENT TURNING AND REPOSITIONING G DEV. receive FDA 510(k) clearance?

PATIENT TURNING AND REPOSITIONING G DEV. received FDA 510(k) clearance on 1977-04-29, under 510(k) number K770499.

Who is the listed applicant for PATIENT TURNING AND REPOSITIONING G DEV.?

The FDA 510(k) record lists Patient Healthguards Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT TURNING AND REPOSITIONING G DEV.?

The FDA product code for PATIENT TURNING AND REPOSITIONING G DEV. is FMR.

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Related Devices (Code: FMR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K871475SOLOLIFT - PATIENT TRANSFER STRETCHERAdel Medical , Ltd.K801796THE COMFORT LIFTGettner Enterprises, Inc.K800373TENDERLIFTCompetent DesignK792318SKIL-CARE TURN AND HOLD PADSkil-Care Corp.

Official Source

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

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