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FDA 510(k)

FLH1768M SERIES HOSPITAL BED

K-Number: K930234 · 1993-07-27

ApplicantBertec Medical, Inc.
Decision Date1993-07-27
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FLH1768M SERIES HOSPITAL BED is the device name listed in this FDA 510(k) record. The listed applicant is Bertec Medical, Inc.. It received FDA 510(k) clearance on 1993-07-27 under 510(k) number K930234. 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 FLH1768M SERIES HOSPITAL BED?

FLH1768M SERIES HOSPITAL BED is a medical device that received FDA 510(k) clearance on 1993-07-27. The listed applicant is Bertec Medical, Inc.. The 510(k) number is K930234.

When did FLH1768M SERIES HOSPITAL BED receive FDA 510(k) clearance?

FLH1768M SERIES HOSPITAL BED received FDA 510(k) clearance on 1993-07-27, under 510(k) number K930234.

Who is the listed applicant for FLH1768M SERIES HOSPITAL BED?

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

What is the FDA product code for FLH1768M SERIES HOSPITAL BED?

The FDA product code for FLH1768M SERIES HOSPITAL BED is FNL.

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Related Devices (Code: FNL)

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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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