SILICONE BILIARY STENT/BILIARY CATHETER
K-Number: K973114 · 1997-09-19
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Device Summary
Frequently Asked Questions
What is the SILICONE BILIARY STENT/BILIARY CATHETER?
SILICONE BILIARY STENT/BILIARY CATHETER is a medical device that received FDA 510(k) clearance on 1997-09-19. The listed applicant is Specialty Surgical Products, Inc.. The 510(k) number is K973114.
When did SILICONE BILIARY STENT/BILIARY CATHETER receive FDA 510(k) clearance?
SILICONE BILIARY STENT/BILIARY CATHETER received FDA 510(k) clearance on 1997-09-19, under 510(k) number K973114.
Who is the listed applicant for SILICONE BILIARY STENT/BILIARY CATHETER?
The FDA 510(k) record lists Specialty Surgical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SILICONE BILIARY STENT/BILIARY CATHETER?
The FDA product code for SILICONE BILIARY STENT/BILIARY CATHETER 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 Specialty Surgical Products, Inc. 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.
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