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FDA 510(k)

nvc

K-Number: K190380 · 2019-03-21

ApplicantNvision Biomedical Technologies, Inc.
Decision Date2019-03-21
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

nvc 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 2019-03-21 under 510(k) number K190380. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the nvc?

nvc is a medical device that received FDA 510(k) clearance on 2019-03-21. The listed applicant is Nvision Biomedical Technologies, Inc.. The 510(k) number is K190380.

When did nvc receive FDA 510(k) clearance?

nvc received FDA 510(k) clearance on 2019-03-21, under 510(k) number K190380.

Who is the listed applicant for nvc?

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 nvc?

The FDA product code for nvc is ODP.

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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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