FDA 510(k)

Bard Mission Disposable Core Biopsy Instrument

K-Number: K171953 · 2017-09-14

Decision Date2017-09-14

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

Bard Mission Disposable Core Biopsy Instrument is the device name listed in this FDA 510(k) record. The listed applicant is Bard Peripheral Vascular, Inc.. It received FDA 510(k) clearance on 2017-09-14 under 510(k) number K171953. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Bard Mission Disposable Core Biopsy Instrument?

Bard Mission Disposable Core Biopsy Instrument is a medical device that received FDA 510(k) clearance on 2017-09-14. The listed applicant is Bard Peripheral Vascular, Inc.. The 510(k) number is K171953.

When did Bard Mission Disposable Core Biopsy Instrument receive FDA 510(k) clearance?

Bard Mission Disposable Core Biopsy Instrument received FDA 510(k) clearance on 2017-09-14, under 510(k) number K171953.

Who is the listed applicant for Bard Mission Disposable Core Biopsy Instrument?

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

What is the FDA product code for Bard Mission Disposable Core Biopsy Instrument?

The FDA product code for Bard Mission Disposable Core Biopsy Instrument is KNW.

Other records listing Bard Peripheral Vascular, Inc. as applicant

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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.