E-Cath STIM acc. Tsui
K-Number: K202699 · 2020-12-29
ApplicantPAJUNK GmbH Medizintechnologie
Decision Date2020-12-29
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
E-Cath STIM acc. Tsui is a medical device manufactured by PAJUNK GmbH Medizintechnologie. It received FDA 510(k) clearance on 2020-12-29 under approval number K202699. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the E-Cath STIM acc. Tsui?
E-Cath STIM acc. Tsui is a medical device that received FDA 510(k) clearance on 2020-12-29. It is manufactured by PAJUNK GmbH Medizintechnologie. The 510(k) number is K202699.
When was E-Cath STIM acc. Tsui approved by the FDA?
E-Cath STIM acc. Tsui received FDA 510(k) clearance on 2020-12-29, under approval number K202699.
What company makes E-Cath STIM acc. Tsui?
E-Cath STIM acc. Tsui is manufactured by PAJUNK GmbH Medizintechnologie.
What is the FDA product code for E-Cath STIM acc. Tsui?
The FDA product code for E-Cath STIM acc. Tsui is CAZ.
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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.