Reprocessed Dynamic Tip Steerable Diagnostic Electrophysiology Catheters
K-Number: K161464 · 2016-09-30
Device Summary
Frequently Asked Questions
What is the Reprocessed Dynamic Tip Steerable Diagnostic Electrophysiology Catheters?
Reprocessed Dynamic Tip Steerable Diagnostic Electrophysiology Catheters is a medical device that received FDA 510(k) clearance on 2016-09-30. It is manufactured by Innovative Health, LLC. The 510(k) number is K161464.
When was Reprocessed Dynamic Tip Steerable Diagnostic Electrophysiology Catheters approved by the FDA?
Reprocessed Dynamic Tip Steerable Diagnostic Electrophysiology Catheters received FDA 510(k) clearance on 2016-09-30, under approval number K161464.
What company makes Reprocessed Dynamic Tip Steerable Diagnostic Electrophysiology Catheters?
Reprocessed Dynamic Tip Steerable Diagnostic Electrophysiology Catheters is manufactured by Innovative Health, LLC.
What is the FDA product code for Reprocessed Dynamic Tip Steerable Diagnostic Electrophysiology Catheters?
The FDA product code for Reprocessed Dynamic Tip Steerable Diagnostic Electrophysiology Catheters is NLH.
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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.