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FDA 510(k)

THE COMFORT LIFT

K-Number: K801796 · 1980-08-13

ApplicantGettner Enterprises, Inc.
Decision Date1980-08-13
Product CodeFMR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE COMFORT LIFT is the device name listed in this FDA 510(k) record. The listed applicant is Gettner Enterprises, Inc.. It received FDA 510(k) clearance on 1980-08-13 under 510(k) number K801796. 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 THE COMFORT LIFT?

THE COMFORT LIFT is a medical device that received FDA 510(k) clearance on 1980-08-13. The listed applicant is Gettner Enterprises, Inc.. The 510(k) number is K801796.

When did THE COMFORT LIFT receive FDA 510(k) clearance?

THE COMFORT LIFT received FDA 510(k) clearance on 1980-08-13, under 510(k) number K801796.

Who is the listed applicant for THE COMFORT LIFT?

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

What is the FDA product code for THE COMFORT LIFT?

The FDA product code for THE COMFORT LIFT 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.K800373TENDERLIFTCompetent DesignK792318SKIL-CARE TURN AND HOLD PADSkil-Care Corp.K770499PATIENT TURNING AND REPOSITIONING G DEV.Patient Healthguards Corp.

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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