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FDA 510(k)

hypodermic Pinpoint™ GT Needle

K-Number: K163437 · 2017-06-23

ApplicantC.R. Bard, Inc.
Decision Date2017-06-23
Product CodePVZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

hypodermic Pinpoint™ GT Needle 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 2017-06-23 under 510(k) number K163437. The device is classified under product code PVZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the hypodermic Pinpoint™ GT Needle?

hypodermic Pinpoint™ GT Needle is a medical device that received FDA 510(k) clearance on 2017-06-23. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K163437.

When did hypodermic Pinpoint™ GT Needle receive FDA 510(k) clearance?

hypodermic Pinpoint™ GT Needle received FDA 510(k) clearance on 2017-06-23, under 510(k) number K163437.

Who is the listed applicant for hypodermic Pinpoint™ GT Needle?

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 hypodermic Pinpoint™ GT Needle?

The FDA product code for hypodermic Pinpoint™ GT Needle is PVZ.

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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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