Reprocessed Electrophysiology Catheter
K-Number: K153153 · 2016-03-14
Device Summary
Frequently Asked Questions
What is the Reprocessed Electrophysiology Catheter?
Reprocessed Electrophysiology Catheter is a medical device that received FDA 510(k) clearance on 2016-03-14. It is manufactured by Innovative Health, LLC. The 510(k) number is K153153.
When was Reprocessed Electrophysiology Catheter approved by the FDA?
Reprocessed Electrophysiology Catheter received FDA 510(k) clearance on 2016-03-14, under approval number K153153.
What company makes Reprocessed Electrophysiology Catheter?
Reprocessed Electrophysiology Catheter is manufactured by Innovative Health, LLC.
What is the FDA product code for Reprocessed Electrophysiology Catheter?
The FDA product code for Reprocessed Electrophysiology Catheter is NLH.
Related Clinical Trials
Other Devices by Innovative Health, LLC
Related Devices (Code: NLH)
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.