Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter
K-Number: K173262 · 2018-03-06
Device Summary
Frequently Asked Questions
What is the Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter?
Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter is a medical device that received FDA 510(k) clearance on 2018-03-06. The listed applicant is Innovative Health, LLC. The 510(k) number is K173262.
When did Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter receive FDA 510(k) clearance?
Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter received FDA 510(k) clearance on 2018-03-06, under 510(k) number K173262.
Who is the listed applicant for Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter?
The FDA 510(k) record lists Innovative Health, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter?
The FDA product code for Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter is OWQ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Innovative Health, LLC as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OWQ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.