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FDA 510(k)

THE VERSA-BED

K-Number: K792298 · 1979-12-20

ApplicantFirst & Ten, Inc.
Decision Date1979-12-20
Product CodeFNJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE VERSA-BED is the device name listed in this FDA 510(k) record. The listed applicant is First & Ten, Inc.. It received FDA 510(k) clearance on 1979-12-20 under 510(k) number K792298. The device is classified under product code FNJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE VERSA-BED?

THE VERSA-BED is a medical device that received FDA 510(k) clearance on 1979-12-20. The listed applicant is First & Ten, Inc.. The 510(k) number is K792298.

When did THE VERSA-BED receive FDA 510(k) clearance?

THE VERSA-BED received FDA 510(k) clearance on 1979-12-20, under 510(k) number K792298.

Who is the listed applicant for THE VERSA-BED?

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

What is the FDA product code for THE VERSA-BED?

The FDA product code for THE VERSA-BED is FNJ.

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Related Devices (Code: FNJ)

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

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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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