LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER
K-Number: K922190 · 1992-10-23
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Device Summary
Frequently Asked Questions
What is the LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER?
LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER is a medical device that received FDA 510(k) clearance on 1992-10-23. The listed applicant is Advanced Surgical, Inc.. The 510(k) number is K922190.
When did LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER receive FDA 510(k) clearance?
LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER received FDA 510(k) clearance on 1992-10-23, under 510(k) number K922190.
Who is the listed applicant for LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER?
The FDA 510(k) record lists Advanced Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER?
The FDA product code for LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER is FMF.
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 Advanced Surgical, 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: FMF)
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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