URETERAL CATHETER HOLDER
K-Number: K912146 · 1991-07-26
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Device Summary
Frequently Asked Questions
What is the URETERAL CATHETER HOLDER?
URETERAL CATHETER HOLDER is a medical device that received FDA 510(k) clearance on 1991-07-26. The listed applicant is Inman Liebelt Corp.. The 510(k) number is K912146.
When did URETERAL CATHETER HOLDER receive FDA 510(k) clearance?
URETERAL CATHETER HOLDER received FDA 510(k) clearance on 1991-07-26, under 510(k) number K912146.
Who is the listed applicant for URETERAL CATHETER HOLDER?
The FDA 510(k) record lists Inman Liebelt Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for URETERAL CATHETER HOLDER?
The FDA product code for URETERAL CATHETER HOLDER is KNY.
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 Inman Liebelt 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: KNY)
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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