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FDA 510(k)

MONTG. TRACHEAL TREPHINE FENE STRATOR

K-Number: K802915 · 1980-12-19

ApplicantBoston Medical Products, Inc.
Decision Date1980-12-19
Product CodeKBF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MONTG. TRACHEAL TREPHINE FENE STRATOR 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 K802915. The device is classified under product code KBF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONTG. TRACHEAL TREPHINE FENE STRATOR?

MONTG. TRACHEAL TREPHINE FENE STRATOR 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 K802915.

When did MONTG. TRACHEAL TREPHINE FENE STRATOR receive FDA 510(k) clearance?

MONTG. TRACHEAL TREPHINE FENE STRATOR received FDA 510(k) clearance on 1980-12-19, under 510(k) number K802915.

Who is the listed applicant for MONTG. TRACHEAL TREPHINE FENE STRATOR?

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 TREPHINE FENE STRATOR?

The FDA product code for MONTG. TRACHEAL TREPHINE FENE STRATOR is KBF.

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Other records listing Boston Medical Products, Inc. as applicant

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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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