FDA 510(k)

NORTON ENDOTRACHEAL

K-Number: K771197 · 1977-08-16

ApplicantV. Mueller O.V. Baxter Healthcare Corp.

Decision Date1977-08-16

Product CodeBTR

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

NORTON ENDOTRACHEAL is the device name listed in this FDA 510(k) record. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. It received FDA 510(k) clearance on 1977-08-16 under 510(k) number K771197. 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 NORTON ENDOTRACHEAL?

NORTON ENDOTRACHEAL is a medical device that received FDA 510(k) clearance on 1977-08-16. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K771197.

When did NORTON ENDOTRACHEAL receive FDA 510(k) clearance?

NORTON ENDOTRACHEAL received FDA 510(k) clearance on 1977-08-16, under 510(k) number K771197.

Who is the listed applicant for NORTON ENDOTRACHEAL?

The FDA 510(k) record lists V. Mueller O.V. Baxter Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NORTON ENDOTRACHEAL?

The FDA product code for NORTON ENDOTRACHEAL is BTR.

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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.