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)

Corvocet Biopsy System

K-Number: K180450 · 2018-03-12

Decision Date2018-03-12
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Corvocet Biopsy System is a medical device manufactured by Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 2018-03-12 under approval number K180450. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Corvocet Biopsy System?

Corvocet Biopsy System is a medical device that received FDA 510(k) clearance on 2018-03-12. It is manufactured by Merit Medical Systems, Inc.. The 510(k) number is K180450.

When was Corvocet Biopsy System approved by the FDA?

Corvocet Biopsy System received FDA 510(k) clearance on 2018-03-12, under approval number K180450.

What company makes Corvocet Biopsy System?

Corvocet Biopsy System is manufactured by Merit Medical Systems, Inc..

What is the FDA product code for Corvocet Biopsy System?

The FDA product code for Corvocet Biopsy System is KNW.

Related Clinical Trials

Other Devices by Merit Medical Systems, Inc.

View all 65 devices →

Related Devices (Code: KNW)

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.