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FDA 510(k)

INVALIFT

K-Number: K910830 · 1992-06-09

ApplicantAmerican Invalift Corp.
Decision Date1992-06-09
Product CodeFRZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INVALIFT is the device name listed in this FDA 510(k) record. The listed applicant is American Invalift Corp.. It received FDA 510(k) clearance on 1992-06-09 under 510(k) number K910830. The device is classified under product code FRZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INVALIFT?

INVALIFT is a medical device that received FDA 510(k) clearance on 1992-06-09. The listed applicant is American Invalift Corp.. The 510(k) number is K910830.

When did INVALIFT receive FDA 510(k) clearance?

INVALIFT received FDA 510(k) clearance on 1992-06-09, under 510(k) number K910830.

Who is the listed applicant for INVALIFT?

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

What is the FDA product code for INVALIFT?

The FDA product code for INVALIFT is FRZ.

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Related Devices (Code: FRZ)

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.

K121929ZEPHYR 'X-SERIES PATIENT TRANSFER SLEDDiacor, Inc.K841728LCI MEDICAL INC AIR/PALLehigh Consolidated IndustriesK834585CELLTRAK-BR&D Systems, Inc.K840796TENDER LIFTING CARELancer Assoc.

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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