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FDA 510(k)

BED, PARAPLEGIC

K-Number: K790049 · 1979-02-27

ApplicantWayne V. Kirkman
Decision Date1979-02-27
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BED, PARAPLEGIC is the device name listed in this FDA 510(k) record. The listed applicant is Wayne V. Kirkman. It received FDA 510(k) clearance on 1979-02-27 under 510(k) number K790049. 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 BED, PARAPLEGIC?

BED, PARAPLEGIC is a medical device that received FDA 510(k) clearance on 1979-02-27. The listed applicant is Wayne V. Kirkman. The 510(k) number is K790049.

When did BED, PARAPLEGIC receive FDA 510(k) clearance?

BED, PARAPLEGIC received FDA 510(k) clearance on 1979-02-27, under 510(k) number K790049.

Who is the listed applicant for BED, PARAPLEGIC?

The FDA 510(k) record lists Wayne V. Kirkman as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BED, PARAPLEGIC?

The FDA product code for BED, PARAPLEGIC is FNL.

Related Clinical Trials

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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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.

K202964iBed Wireless with iBed MobileStryker CorporationK103536IBED WIRELESS WITH IBED AWARENESSStryker CorporationK982783VAIL 1000 ENCLOSED BEDVail Products, Inc.K974296MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BEDInvacare Corp.K974254BENEFIT B3--- SERIESM.C. Healthcare Products, Inc.K972115VOLKER HOSPITAL BED, MODEL K960Volker Healthcare, Inc.

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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