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)

CN ENDOTRACHEAL TUBE HOLDER

K-Number: K921698 · 1992-09-15

Decision Date1992-09-15
Product CodeCBH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CN ENDOTRACHEAL TUBE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is N-C-N Products Co.. It received FDA 510(k) clearance on 1992-09-15 under 510(k) number K921698. The device is classified under product code CBH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CN ENDOTRACHEAL TUBE HOLDER?

CN ENDOTRACHEAL TUBE HOLDER is a medical device that received FDA 510(k) clearance on 1992-09-15. The listed applicant is N-C-N Products Co.. The 510(k) number is K921698.

When did CN ENDOTRACHEAL TUBE HOLDER receive FDA 510(k) clearance?

CN ENDOTRACHEAL TUBE HOLDER received FDA 510(k) clearance on 1992-09-15, under 510(k) number K921698.

Who is the listed applicant for CN ENDOTRACHEAL TUBE HOLDER?

The FDA 510(k) record lists N-C-N Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CN ENDOTRACHEAL TUBE HOLDER?

The FDA product code for CN ENDOTRACHEAL TUBE HOLDER is CBH.

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: CBH)

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.

↑