FDA 510(k)

INSTRUMENT CURNETT MINI-CONER BIOPSY

K-Number: K781767 · 1978-12-07

Decision Date1978-12-07

Product CodeKOH

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

INSTRUMENT CURNETT MINI-CONER BIOPSY is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1978-12-07 under 510(k) number K781767. The device is classified under product code KOH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENT CURNETT MINI-CONER BIOPSY?

INSTRUMENT CURNETT MINI-CONER BIOPSY is a medical device that received FDA 510(k) clearance on 1978-12-07. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K781767.

When did INSTRUMENT CURNETT MINI-CONER BIOPSY receive FDA 510(k) clearance?

INSTRUMENT CURNETT MINI-CONER BIOPSY received FDA 510(k) clearance on 1978-12-07, under 510(k) number K781767.

Who is the listed applicant for INSTRUMENT CURNETT MINI-CONER BIOPSY?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSTRUMENT CURNETT MINI-CONER BIOPSY?

The FDA product code for INSTRUMENT CURNETT MINI-CONER BIOPSY is KOH.

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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.