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FDA 510(k)

THE HENLEY BOARD S.I.D. SPINAL IMMOBILIZATION DEVI

K-Number: K852100 · 1985-07-24

ApplicantHenley Board, Inc.
Decision Date1985-07-24
Product CodeFPD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

THE HENLEY BOARD S.I.D. SPINAL IMMOBILIZATION DEVI is the device name listed in this FDA 510(k) record. The listed applicant is Henley Board, Inc.. It received FDA 510(k) clearance on 1985-07-24 under 510(k) number K852100. The device is classified under product code FPD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE HENLEY BOARD S.I.D. SPINAL IMMOBILIZATION DEVI?

THE HENLEY BOARD S.I.D. SPINAL IMMOBILIZATION DEVI is a medical device that received FDA 510(k) clearance on 1985-07-24. The listed applicant is Henley Board, Inc.. The 510(k) number is K852100.

When did THE HENLEY BOARD S.I.D. SPINAL IMMOBILIZATION DEVI receive FDA 510(k) clearance?

THE HENLEY BOARD S.I.D. SPINAL IMMOBILIZATION DEVI received FDA 510(k) clearance on 1985-07-24, under 510(k) number K852100.

Who is the listed applicant for THE HENLEY BOARD S.I.D. SPINAL IMMOBILIZATION DEVI?

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

What is the FDA product code for THE HENLEY BOARD S.I.D. SPINAL IMMOBILIZATION DEVI?

The FDA product code for THE HENLEY BOARD S.I.D. SPINAL IMMOBILIZATION DEVI is FPD.

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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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