ValPro 2 Plus, VaPro 2 Plus Pocket
K-Number: K183253 · 2018-12-18
ApplicantHollister Incorporated
Decision Date2018-12-18
Product CodeGBM
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
ValPro 2 Plus, VaPro 2 Plus Pocket is a medical device manufactured by Hollister Incorporated. It received FDA 510(k) clearance on 2018-12-18 under approval number K183253. 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 ValPro 2 Plus, VaPro 2 Plus Pocket?
ValPro 2 Plus, VaPro 2 Plus Pocket is a medical device that received FDA 510(k) clearance on 2018-12-18. It is manufactured by Hollister Incorporated. The 510(k) number is K183253.
When was ValPro 2 Plus, VaPro 2 Plus Pocket approved by the FDA?
ValPro 2 Plus, VaPro 2 Plus Pocket received FDA 510(k) clearance on 2018-12-18, under approval number K183253.
What company makes ValPro 2 Plus, VaPro 2 Plus Pocket?
ValPro 2 Plus, VaPro 2 Plus Pocket is manufactured by Hollister Incorporated.
What is the FDA product code for ValPro 2 Plus, VaPro 2 Plus Pocket?
The FDA product code for ValPro 2 Plus, VaPro 2 Plus Pocket 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.