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FDA 510(k)

EASY ACCESS BED

K-Number: K911893 · 1991-11-22

ApplicantWillis Therapeutic Innovations, Inc.
Decision Date1991-11-22
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EASY ACCESS BED is the device name listed in this FDA 510(k) record. The listed applicant is Willis Therapeutic Innovations, Inc.. It received FDA 510(k) clearance on 1991-11-22 under 510(k) number K911893. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASY ACCESS BED?

EASY ACCESS BED is a medical device that received FDA 510(k) clearance on 1991-11-22. The listed applicant is Willis Therapeutic Innovations, Inc.. The 510(k) number is K911893.

When did EASY ACCESS BED receive FDA 510(k) clearance?

EASY ACCESS BED received FDA 510(k) clearance on 1991-11-22, under 510(k) number K911893.

Who is the listed applicant for EASY ACCESS BED?

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

What is the FDA product code for EASY ACCESS BED?

The FDA product code for EASY ACCESS BED is FNL.

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Related Devices (Code: FNL)

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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