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FDA 510(k)

Bard Mission Disposable Core Biopsy Instrument

K-Number: K171953 · 2017-09-14

ApplicantBard Peripheral Vascular, Inc.
Decision Date2017-09-14
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Bard Mission Disposable Core Biopsy Instrument is a medical device manufactured by Bard Peripheral Vascular, Inc.. It received FDA 510(k) clearance on 2017-09-14 under approval 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. It is manufactured by Bard Peripheral Vascular, Inc.. The 510(k) number is K171953.

When was Bard Mission Disposable Core Biopsy Instrument approved by the FDA?

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

What company makes Bard Mission Disposable Core Biopsy Instrument?

Bard Mission Disposable Core Biopsy Instrument is manufactured by Bard Peripheral Vascular, Inc..

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.

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Related Devices (Code: KNW)

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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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