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FDA 510(k)

VACORA VACUUM ASSISTED BIOPSY SYSTEM

K-Number: K082681 · 2008-10-15

ApplicantC.R. Bard, Inc.
Decision Date2008-10-15
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VACORA VACUUM ASSISTED BIOPSY SYSTEM 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 2008-10-15 under 510(k) number K082681. 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 VACORA VACUUM ASSISTED BIOPSY SYSTEM?

VACORA VACUUM ASSISTED BIOPSY SYSTEM is a medical device that received FDA 510(k) clearance on 2008-10-15. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K082681.

When did VACORA VACUUM ASSISTED BIOPSY SYSTEM receive FDA 510(k) clearance?

VACORA VACUUM ASSISTED BIOPSY SYSTEM received FDA 510(k) clearance on 2008-10-15, under 510(k) number K082681.

Who is the listed applicant for VACORA VACUUM ASSISTED BIOPSY SYSTEM?

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 VACORA VACUUM ASSISTED BIOPSY SYSTEM?

The FDA product code for VACORA VACUUM ASSISTED BIOPSY SYSTEM 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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