URETERAL CATHETER
K-Number: K923729 · 1993-12-07
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Device Summary
Frequently Asked Questions
What is the URETERAL CATHETER?
URETERAL CATHETER is a medical device that received FDA 510(k) clearance on 1993-12-07. The listed applicant is Cook Urological, Inc.. The 510(k) number is K923729.
When did URETERAL CATHETER receive FDA 510(k) clearance?
URETERAL CATHETER received FDA 510(k) clearance on 1993-12-07, under 510(k) number K923729.
Who is the listed applicant for URETERAL CATHETER?
The FDA 510(k) record lists Cook Urological, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for URETERAL CATHETER?
The FDA product code for URETERAL CATHETER is EYB.
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 Cook Urological, 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: EYB)
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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