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FDA 510(k)

COT, FOLDING HOSPITAL ALUMINUM - MANUAL BED

K-Number: K861678 · 1986-05-08

ApplicantSierra Corp.
Decision Date1986-05-08
Product CodeFNJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COT, FOLDING HOSPITAL ALUMINUM - MANUAL BED is the device name listed in this FDA 510(k) record. The listed applicant is Sierra Corp.. It received FDA 510(k) clearance on 1986-05-08 under 510(k) number K861678. The device is classified under product code FNJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COT, FOLDING HOSPITAL ALUMINUM - MANUAL BED?

COT, FOLDING HOSPITAL ALUMINUM - MANUAL BED is a medical device that received FDA 510(k) clearance on 1986-05-08. The listed applicant is Sierra Corp.. The 510(k) number is K861678.

When did COT, FOLDING HOSPITAL ALUMINUM - MANUAL BED receive FDA 510(k) clearance?

COT, FOLDING HOSPITAL ALUMINUM - MANUAL BED received FDA 510(k) clearance on 1986-05-08, under 510(k) number K861678.

Who is the listed applicant for COT, FOLDING HOSPITAL ALUMINUM - MANUAL BED?

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

What is the FDA product code for COT, FOLDING HOSPITAL ALUMINUM - MANUAL BED?

The FDA product code for COT, FOLDING HOSPITAL ALUMINUM - MANUAL BED is FNJ.

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.

Related Devices (Code: FNJ)

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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