VaPro Plus Pocket, VaPro Plus
K-Number: K193148 · 2019-12-13
ApplicantHollister Incorporated
Decision Date2019-12-13
Product CodeGBM
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
VaPro Plus Pocket, VaPro Plus is a medical device manufactured by Hollister Incorporated. It received FDA 510(k) clearance on 2019-12-13 under approval number K193148. The device is classified under product code GBM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the VaPro Plus Pocket, VaPro Plus?
VaPro Plus Pocket, VaPro Plus is a medical device that received FDA 510(k) clearance on 2019-12-13. It is manufactured by Hollister Incorporated. The 510(k) number is K193148.
When was VaPro Plus Pocket, VaPro Plus approved by the FDA?
VaPro Plus Pocket, VaPro Plus received FDA 510(k) clearance on 2019-12-13, under approval number K193148.
What company makes VaPro Plus Pocket, VaPro Plus?
VaPro Plus Pocket, VaPro Plus is manufactured by Hollister Incorporated.
What is the FDA product code for VaPro Plus Pocket, VaPro Plus?
The FDA product code for VaPro Plus Pocket, VaPro Plus is GBM.
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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.