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FDA 510(k)

MONTG. TRACHEAL CANNULA

K-Number: K802916 · 1980-12-19

ApplicantBoston Medical Products, Inc.
Decision Date1980-12-19
Product CodeBTO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MONTG. TRACHEAL CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Boston Medical Products, Inc.. It received FDA 510(k) clearance on 1980-12-19 under 510(k) number K802916. The device is classified under product code BTO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONTG. TRACHEAL CANNULA?

MONTG. TRACHEAL CANNULA is a medical device that received FDA 510(k) clearance on 1980-12-19. The listed applicant is Boston Medical Products, Inc.. The 510(k) number is K802916.

When did MONTG. TRACHEAL CANNULA receive FDA 510(k) clearance?

MONTG. TRACHEAL CANNULA received FDA 510(k) clearance on 1980-12-19, under 510(k) number K802916.

Who is the listed applicant for MONTG. TRACHEAL CANNULA?

The FDA 510(k) record lists Boston Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MONTG. TRACHEAL CANNULA?

The FDA product code for MONTG. TRACHEAL CANNULA is BTO.

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Related Devices (Code: BTO)

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.

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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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