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FDA 510(k)

BED BOARD

K-Number: K780230 · 1978-02-28

ApplicantBiomet, Inc.
Decision Date1978-02-28
Product CodeFPS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BED BOARD is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1978-02-28 under 510(k) number K780230. The device is classified under product code FPS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BED BOARD?

BED BOARD is a medical device that received FDA 510(k) clearance on 1978-02-28. The listed applicant is Biomet, Inc.. The 510(k) number is K780230.

When did BED BOARD receive FDA 510(k) clearance?

BED BOARD received FDA 510(k) clearance on 1978-02-28, under 510(k) number K780230.

Who is the listed applicant for BED BOARD?

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

What is the FDA product code for BED BOARD?

The FDA product code for BED BOARD is FPS.

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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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