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FDA 510(k)

nva, nvp, and nvt

K-Number: K193645 · 2020-01-13

ApplicantNvision Biomedical Technologies, Inc.
Decision Date2020-01-13
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

nva, nvp, and nvt is the device name listed in this FDA 510(k) record. The listed applicant is Nvision Biomedical Technologies, Inc.. It received FDA 510(k) clearance on 2020-01-13 under 510(k) 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. The listed applicant is Nvision Biomedical Technologies, Inc.. The 510(k) number is K193645.

When did nva, nvp, and nvt receive FDA 510(k) clearance?

nva, nvp, and nvt received FDA 510(k) clearance on 2020-01-13, under 510(k) number K193645.

Who is the listed applicant for nva, nvp, and nvt?

The FDA 510(k) record lists Nvision Biomedical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

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.

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