Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

nvc

K-Number: K190380 · 2019-03-21

Decision Date2019-03-21
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

nvc is a medical device manufactured by Nvision Biomedical Technologies, Inc.. It received FDA 510(k) clearance on 2019-03-21 under approval 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. It is manufactured by Nvision Biomedical Technologies, Inc.. The 510(k) number is K190380.

When was nvc approved by the FDA?

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

What company makes nvc?

nvc is manufactured by Nvision Biomedical Technologies, Inc..

What is the FDA product code for nvc?

The FDA product code for nvc is ODP.

Other Devices by Nvision Biomedical Technologies, Inc.

View all 24 devices →

Related Devices (Code: ODP)

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.