Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

FOLDING HOSPITAL COT NSN 6530-00-299-8517

K-Number: K881043 · 1988-04-12

Decision Date1988-04-12
Product CodeFNJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FOLDING HOSPITAL COT NSN 6530-00-299-8517 is the device name listed in this FDA 510(k) record. The listed applicant is Junkin Safety Appliance Co., Inc.. It received FDA 510(k) clearance on 1988-04-12 under 510(k) number K881043. 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 FOLDING HOSPITAL COT NSN 6530-00-299-8517?

FOLDING HOSPITAL COT NSN 6530-00-299-8517 is a medical device that received FDA 510(k) clearance on 1988-04-12. The listed applicant is Junkin Safety Appliance Co., Inc.. The 510(k) number is K881043.

When did FOLDING HOSPITAL COT NSN 6530-00-299-8517 receive FDA 510(k) clearance?

FOLDING HOSPITAL COT NSN 6530-00-299-8517 received FDA 510(k) clearance on 1988-04-12, under 510(k) number K881043.

Who is the listed applicant for FOLDING HOSPITAL COT NSN 6530-00-299-8517?

The FDA 510(k) record lists Junkin Safety Appliance Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FOLDING HOSPITAL COT NSN 6530-00-299-8517?

The FDA product code for FOLDING HOSPITAL COT NSN 6530-00-299-8517 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.

Other records listing Junkin Safety Appliance Co., Inc. 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: 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑