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)

Virtual C DRF Digital Imaging System

K-Number: K211191 · 2021-06-24

Decision Date2021-06-24
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Virtual C DRF Digital Imaging System is a medical device manufactured by Portavision Medical, LLC. It received FDA 510(k) clearance on 2021-06-24 under approval number K211191. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Virtual C DRF Digital Imaging System?

Virtual C DRF Digital Imaging System is a medical device that received FDA 510(k) clearance on 2021-06-24. It is manufactured by Portavision Medical, LLC. The 510(k) number is K211191.

When was Virtual C DRF Digital Imaging System approved by the FDA?

Virtual C DRF Digital Imaging System received FDA 510(k) clearance on 2021-06-24, under approval number K211191.

What company makes Virtual C DRF Digital Imaging System?

Virtual C DRF Digital Imaging System is manufactured by Portavision Medical, LLC.

What is the FDA product code for Virtual C DRF Digital Imaging System?

The FDA product code for Virtual C DRF Digital Imaging System is OWB.

Related Clinical Trials

Related PubMed Literature

Other Devices by Portavision Medical, LLC

Related Devices (Code: OWB)

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.