Sapphire NC Plus Coronary Dilatation Catheter
K-Number: K192344 · 2019-09-19
Device Summary
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.
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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.