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FDA 510(k)

ENDOTRACHAEL TUBE AND HOLDER

K-Number: K760998 · 1976-11-19

Decision Date1976-11-19
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ENDOTRACHAEL TUBE AND HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Mcgaw Respiratory Therapy. It received FDA 510(k) clearance on 1976-11-19 under 510(k) number K760998. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOTRACHAEL TUBE AND HOLDER?

ENDOTRACHAEL TUBE AND HOLDER is a medical device that received FDA 510(k) clearance on 1976-11-19. The listed applicant is Mcgaw Respiratory Therapy. The 510(k) number is K760998.

When did ENDOTRACHAEL TUBE AND HOLDER receive FDA 510(k) clearance?

ENDOTRACHAEL TUBE AND HOLDER received FDA 510(k) clearance on 1976-11-19, under 510(k) number K760998.

Who is the listed applicant for ENDOTRACHAEL TUBE AND HOLDER?

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

What is the FDA product code for ENDOTRACHAEL TUBE AND HOLDER?

The FDA product code for ENDOTRACHAEL TUBE AND HOLDER is BTR.

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 Mcgaw Respiratory Therapy 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.

View all 8 devices →

Related Devices (Code: BTR)

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.

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