SCUBA BILIARY STENT SYSTEM
K-Number: K092352 · 2010-03-16
Advertisement
Device Summary
Frequently Asked Questions
What is the SCUBA BILIARY STENT SYSTEM?
SCUBA BILIARY STENT SYSTEM is a medical device that received FDA 510(k) clearance on 2010-03-16. The listed applicant is Invatec S.P.A.. The 510(k) number is K092352.
When did SCUBA BILIARY STENT SYSTEM receive FDA 510(k) clearance?
SCUBA BILIARY STENT SYSTEM received FDA 510(k) clearance on 2010-03-16, under 510(k) number K092352.
Who is the listed applicant for SCUBA BILIARY STENT SYSTEM?
The FDA 510(k) record lists Invatec S.P.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SCUBA BILIARY STENT SYSTEM?
The FDA product code for SCUBA BILIARY STENT SYSTEM is FGE.
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 Invatec S.P.A. 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: FGE)
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.
Advertisement