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FDA 510(k)

TENDERLIFT

K-Number: K800373 · 1980-03-12

ApplicantCompetent Design
Decision Date1980-03-12
Product CodeFMR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TENDERLIFT is the device name listed in this FDA 510(k) record. The listed applicant is Competent Design. It received FDA 510(k) clearance on 1980-03-12 under 510(k) number K800373. 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 TENDERLIFT?

TENDERLIFT is a medical device that received FDA 510(k) clearance on 1980-03-12. The listed applicant is Competent Design. The 510(k) number is K800373.

When did TENDERLIFT receive FDA 510(k) clearance?

TENDERLIFT received FDA 510(k) clearance on 1980-03-12, under 510(k) number K800373.

Who is the listed applicant for TENDERLIFT?

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

What is the FDA product code for TENDERLIFT?

The FDA product code for TENDERLIFT 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.K792318SKIL-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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