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 a medical device manufactured by C.R. Bard, Inc.. It received FDA 510(k) clearance on 2017-06-23 under approval 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. It is manufactured by C.R. Bard, Inc.. The 510(k) number is K163437.
When was hypodermic Pinpoint GT Needle approved by the FDA?
hypodermic Pinpoint GT Needle received FDA 510(k) clearance on 2017-06-23, under approval number K163437.
What company makes hypodermic Pinpoint GT Needle?
hypodermic Pinpoint GT Needle is manufactured by C.R. Bard, Inc..
What is the FDA product code for hypodermic Pinpoint GT Needle?
The FDA product code for hypodermic Pinpoint GT Needle is PVZ.
Related Clinical Trials
Other Devices by C.R. Bard, Inc.
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.