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FDA 510(k)

THE TUCKER SLING

K-Number: K932636 · 1994-01-26

ApplicantTucker Designs, Ltd.
Decision Date1994-01-26
Product CodeFRP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE TUCKER SLING is the device name listed in this FDA 510(k) record. The listed applicant is Tucker Designs, Ltd.. It received FDA 510(k) clearance on 1994-01-26 under 510(k) number K932636. The device is classified under product code FRP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE TUCKER SLING?

THE TUCKER SLING is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Tucker Designs, Ltd.. The 510(k) number is K932636.

When did THE TUCKER SLING receive FDA 510(k) clearance?

THE TUCKER SLING received FDA 510(k) clearance on 1994-01-26, under 510(k) number K932636.

Who is the listed applicant for THE TUCKER SLING?

The FDA 510(k) record lists Tucker Designs, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE TUCKER SLING?

The FDA product code for THE TUCKER SLING is FRP.

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Related Devices (Code: FRP)

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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