SOEHENDRA BILIARY DILATING CATHETER-SBDC-7
K-Number: K851960 · 1985-07-29
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Device Summary
Frequently Asked Questions
What is the SOEHENDRA BILIARY DILATING CATHETER-SBDC-7?
SOEHENDRA BILIARY DILATING CATHETER-SBDC-7 is a medical device that received FDA 510(k) clearance on 1985-07-29. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K851960.
When did SOEHENDRA BILIARY DILATING CATHETER-SBDC-7 receive FDA 510(k) clearance?
SOEHENDRA BILIARY DILATING CATHETER-SBDC-7 received FDA 510(k) clearance on 1985-07-29, under 510(k) number K851960.
Who is the listed applicant for SOEHENDRA BILIARY DILATING CATHETER-SBDC-7?
The FDA 510(k) record lists Wilson-Cook Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SOEHENDRA BILIARY DILATING CATHETER-SBDC-7?
The FDA product code for SOEHENDRA BILIARY DILATING CATHETER-SBDC-7 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 Wilson-Cook Medical, 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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