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)

Sapphire NC Plus Coronary Dilatation Catheter

K-Number: K192344 · 2019-09-19

Decision Date2019-09-19
Product CodeLOX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Sapphire NC Plus Coronary Dilatation Catheter is a medical device manufactured by Orbusneich Medical Trading, Inc.. It received FDA 510(k) clearance on 2019-09-19 under approval number K192344. The device is classified under product code LOX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sapphire NC Plus Coronary Dilatation Catheter?

Sapphire NC Plus Coronary Dilatation Catheter is a medical device that received FDA 510(k) clearance on 2019-09-19. It is manufactured by Orbusneich Medical Trading, Inc.. The 510(k) number is K192344.

When was Sapphire NC Plus Coronary Dilatation Catheter approved by the FDA?

Sapphire NC Plus Coronary Dilatation Catheter received FDA 510(k) clearance on 2019-09-19, under approval number K192344.

What company makes Sapphire NC Plus Coronary Dilatation Catheter?

Sapphire NC Plus Coronary Dilatation Catheter is manufactured by Orbusneich Medical Trading, Inc..

What is the FDA product code for Sapphire NC Plus Coronary Dilatation Catheter?

The FDA product code for Sapphire NC Plus Coronary Dilatation Catheter is LOX.

Related Clinical Trials

Other Devices by Orbusneich Medical Trading, Inc.

View all 7 devices →

Related Devices (Code: LOX)

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.