nva, nvp, and nvt
K-Number: K162426 · 2016-09-29
ApplicantNvision Biomedical Technologies, LLC
Decision Date2016-09-29
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
nva, nvp, and nvt is a medical device manufactured by Nvision Biomedical Technologies, LLC. It received FDA 510(k) clearance on 2016-09-29 under approval number K162426. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the nva, nvp, and nvt?
nva, nvp, and nvt is a medical device that received FDA 510(k) clearance on 2016-09-29. It is manufactured by Nvision Biomedical Technologies, LLC. The 510(k) number is K162426.
When was nva, nvp, and nvt approved by the FDA?
nva, nvp, and nvt received FDA 510(k) clearance on 2016-09-29, under approval number K162426.
What company makes nva, nvp, and nvt?
nva, nvp, and nvt is manufactured by Nvision Biomedical Technologies, LLC.
What is the FDA product code for nva, nvp, and nvt?
The FDA product code for nva, nvp, and nvt is MAX.
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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.