Dannik Titanium Ligation Clip
K-Number: K192711 · 2019-12-20
Device Summary
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. The listed applicant is Dannik. The 510(k) number is K192711.
When did Dannik Titanium Ligation Clip receive FDA 510(k) clearance?
Dannik Titanium Ligation Clip received FDA 510(k) clearance on 2019-12-20, under 510(k) number K192711.
Who is the listed applicant for Dannik Titanium Ligation Clip?
The FDA 510(k) record lists Dannik as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dannik Titanium Ligation Clip?
The FDA product code for Dannik Titanium Ligation Clip is FZP.
Other records listing Dannik 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: FZP)
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.