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FDA 510(k)

BARD BIOPTY-CUT BIOPSY NEEDLE WITH SPACER

K-Number: K910720 · 1991-06-10

ApplicantC.R. Bard, Inc.
Decision Date1991-06-10
Product CodeFCG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BARD BIOPTY-CUT BIOPSY NEEDLE WITH SPACER 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 1991-06-10 under 510(k) number K910720. The device is classified under product code FCG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD BIOPTY-CUT BIOPSY NEEDLE WITH SPACER?

BARD BIOPTY-CUT BIOPSY NEEDLE WITH SPACER is a medical device that received FDA 510(k) clearance on 1991-06-10. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K910720.

When did BARD BIOPTY-CUT BIOPSY NEEDLE WITH SPACER receive FDA 510(k) clearance?

BARD BIOPTY-CUT BIOPSY NEEDLE WITH SPACER received FDA 510(k) clearance on 1991-06-10, under 510(k) number K910720.

Who is the listed applicant for BARD BIOPTY-CUT BIOPSY NEEDLE WITH SPACER?

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 BARD BIOPTY-CUT BIOPSY NEEDLE WITH SPACER?

The FDA product code for BARD BIOPTY-CUT BIOPSY NEEDLE WITH SPACER is FCG.

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Related Devices (Code: FCG)

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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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