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)

Small VBR™

K-Number: K192117 · 2019-11-01

Decision Date2019-11-01
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Small VBR™ is a medical device manufactured by Ulrich GmbH & Co. KG. It received FDA 510(k) clearance on 2019-11-01 under approval number K192117. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Small VBR™?

Small VBR™ is a medical device that received FDA 510(k) clearance on 2019-11-01. It is manufactured by Ulrich GmbH & Co. KG. The 510(k) number is K192117.

When was Small VBR™ approved by the FDA?

Small VBR™ received FDA 510(k) clearance on 2019-11-01, under approval number K192117.

What company makes Small VBR™?

Small VBR™ is manufactured by Ulrich GmbH & Co. KG.

What is the FDA product code for Small VBR™?

The FDA product code for Small VBR™ is MQP.

Other Devices by Ulrich GmbH & Co. KG

View all 11 devices →

Related Devices (Code: MQP)

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.