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FDA 510(k)

BACK REST, LITTER, NON-ADJUSTABLE

K-Number: K863686 · 1987-01-20

Decision Date1987-01-20
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BACK REST, LITTER, NON-ADJUSTABLE is the device name listed in this FDA 510(k) record. The listed applicant is Brenner Metal Prod Corp.. It received FDA 510(k) clearance on 1987-01-20 under 510(k) number K863686. The device is classified under product code FPP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BACK REST, LITTER, NON-ADJUSTABLE?

BACK REST, LITTER, NON-ADJUSTABLE is a medical device that received FDA 510(k) clearance on 1987-01-20. The listed applicant is Brenner Metal Prod Corp.. The 510(k) number is K863686.

When did BACK REST, LITTER, NON-ADJUSTABLE receive FDA 510(k) clearance?

BACK REST, LITTER, NON-ADJUSTABLE received FDA 510(k) clearance on 1987-01-20, under 510(k) number K863686.

Who is the listed applicant for BACK REST, LITTER, NON-ADJUSTABLE?

The FDA 510(k) record lists Brenner Metal Prod Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BACK REST, LITTER, NON-ADJUSTABLE?

The FDA product code for BACK REST, LITTER, NON-ADJUSTABLE is FPP.

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.

Other records listing Brenner Metal Prod Corp. as applicant

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.

Related Devices (Code: FPP)

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.

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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