BAXTER LAPAROSCOPIC CHOLANGIOGRAPHY CATHETERS
K-Number: K905707 · 1991-02-13
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Device Summary
Frequently Asked Questions
What is the BAXTER LAPAROSCOPIC CHOLANGIOGRAPHY CATHETERS?
BAXTER LAPAROSCOPIC CHOLANGIOGRAPHY CATHETERS is a medical device that received FDA 510(k) clearance on 1991-02-13. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K905707.
When did BAXTER LAPAROSCOPIC CHOLANGIOGRAPHY CATHETERS receive FDA 510(k) clearance?
BAXTER LAPAROSCOPIC CHOLANGIOGRAPHY CATHETERS received FDA 510(k) clearance on 1991-02-13, under 510(k) number K905707.
Who is the listed applicant for BAXTER LAPAROSCOPIC CHOLANGIOGRAPHY CATHETERS?
The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BAXTER LAPAROSCOPIC CHOLANGIOGRAPHY CATHETERS?
The FDA product code for BAXTER LAPAROSCOPIC CHOLANGIOGRAPHY CATHETERS 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 Baxter Healthcare Corp 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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