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FDA 510(k)

LIFELIFT MODELS ONE AND TWO

K-Number: K792601 · 1979-12-31

ApplicantCorda Int'L Holiday, Inc.
Decision Date1979-12-31
Product CodeFSA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIFELIFT MODELS ONE AND TWO is the device name listed in this FDA 510(k) record. The listed applicant is Corda Int'L Holiday, Inc.. It received FDA 510(k) clearance on 1979-12-31 under 510(k) number K792601. The device is classified under product code FSA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFELIFT MODELS ONE AND TWO?

LIFELIFT MODELS ONE AND TWO is a medical device that received FDA 510(k) clearance on 1979-12-31. The listed applicant is Corda Int'L Holiday, Inc.. The 510(k) number is K792601.

When did LIFELIFT MODELS ONE AND TWO receive FDA 510(k) clearance?

LIFELIFT MODELS ONE AND TWO received FDA 510(k) clearance on 1979-12-31, under 510(k) number K792601.

Who is the listed applicant for LIFELIFT MODELS ONE AND TWO?

The FDA 510(k) record lists Corda Int'L Holiday, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFELIFT MODELS ONE AND TWO?

The FDA product code for LIFELIFT MODELS ONE AND TWO is FSA.

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Related Devices (Code: FSA)

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.

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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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