Dannik Titanium Ligation Clip
K-Number: K192711 · 2019-12-20
ApplicantDannik
Decision Date2019-12-20
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Dannik Titanium Ligation Clip is a medical device manufactured by Dannik. It received FDA 510(k) clearance on 2019-12-20 under approval number K192711. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Dannik Titanium Ligation Clip?
Dannik Titanium Ligation Clip is a medical device that received FDA 510(k) clearance on 2019-12-20. It is manufactured by Dannik. The 510(k) number is K192711.
When was Dannik Titanium Ligation Clip approved by the FDA?
Dannik Titanium Ligation Clip received FDA 510(k) clearance on 2019-12-20, under approval number K192711.
What company makes Dannik Titanium Ligation Clip?
Dannik Titanium Ligation Clip is manufactured by Dannik.
What is the FDA product code for Dannik Titanium Ligation Clip?
The FDA product code for Dannik Titanium Ligation Clip is FZP.
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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.