CHOLANGIOGRAPHY/CHOLANGIOSCOPY/LIHOPAXY SYSTEM
K-Number: K913986 · 1992-01-28
Advertisement
Device Summary
Frequently Asked Questions
What is the CHOLANGIOGRAPHY/CHOLANGIOSCOPY/LIHOPAXY SYSTEM?
CHOLANGIOGRAPHY/CHOLANGIOSCOPY/LIHOPAXY SYSTEM is a medical device that received FDA 510(k) clearance on 1992-01-28. The listed applicant is Medical Dynamics, Inc.. The 510(k) number is K913986.
When did CHOLANGIOGRAPHY/CHOLANGIOSCOPY/LIHOPAXY SYSTEM receive FDA 510(k) clearance?
CHOLANGIOGRAPHY/CHOLANGIOSCOPY/LIHOPAXY SYSTEM received FDA 510(k) clearance on 1992-01-28, under 510(k) number K913986.
Who is the listed applicant for CHOLANGIOGRAPHY/CHOLANGIOSCOPY/LIHOPAXY SYSTEM?
The FDA 510(k) record lists Medical Dynamics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHOLANGIOGRAPHY/CHOLANGIOSCOPY/LIHOPAXY SYSTEM?
The FDA product code for CHOLANGIOGRAPHY/CHOLANGIOSCOPY/LIHOPAXY 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 Medical Dynamics, 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.
Advertisement