Rusch Intermittent Urethral Catheters
K-Number: K173596 · 2018-01-29
ApplicantTeleflex Medical
Decision Date2018-01-29
Product CodeEZC
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Rusch Intermittent Urethral Catheters is a medical device manufactured by Teleflex Medical. It received FDA 510(k) clearance on 2018-01-29 under approval number K173596. The device is classified under product code EZC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Rusch Intermittent Urethral Catheters?
Rusch Intermittent Urethral Catheters is a medical device that received FDA 510(k) clearance on 2018-01-29. It is manufactured by Teleflex Medical. The 510(k) number is K173596.
When was Rusch Intermittent Urethral Catheters approved by the FDA?
Rusch Intermittent Urethral Catheters received FDA 510(k) clearance on 2018-01-29, under approval number K173596.
What company makes Rusch Intermittent Urethral Catheters?
Rusch Intermittent Urethral Catheters is manufactured by Teleflex Medical.
What is the FDA product code for Rusch Intermittent Urethral Catheters?
The FDA product code for Rusch Intermittent Urethral Catheters is EZC.
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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.