nva, nvp, and nvt
K-Number: K193645 · 2020-01-13
Decision Date2020-01-13
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
nva, nvp, and nvt is a medical device manufactured by Nvision Biomedical Technologies, Inc.. It received FDA 510(k) clearance on 2020-01-13 under approval number K193645. 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 2020-01-13. It is manufactured by Nvision Biomedical Technologies, Inc.. The 510(k) number is K193645.
When was nva, nvp, and nvt approved by the FDA?
nva, nvp, and nvt received FDA 510(k) clearance on 2020-01-13, under approval number K193645.
What company makes nva, nvp, and nvt?
nva, nvp, and nvt is manufactured by Nvision Biomedical Technologies, Inc..
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.