TUBEGRIPPER, UROLOGICAL CATHETER & ACCESSORY
K-Number: K863958 · 1986-11-04
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Device Summary
Frequently Asked Questions
What is the TUBEGRIPPER, UROLOGICAL CATHETER & ACCESSORY?
TUBEGRIPPER, UROLOGICAL CATHETER & ACCESSORY is a medical device that received FDA 510(k) clearance on 1986-11-04. The listed applicant is Cathaid, Inc.. The 510(k) number is K863958.
When did TUBEGRIPPER, UROLOGICAL CATHETER & ACCESSORY receive FDA 510(k) clearance?
TUBEGRIPPER, UROLOGICAL CATHETER & ACCESSORY received FDA 510(k) clearance on 1986-11-04, under 510(k) number K863958.
Who is the listed applicant for TUBEGRIPPER, UROLOGICAL CATHETER & ACCESSORY?
The FDA 510(k) record lists Cathaid, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TUBEGRIPPER, UROLOGICAL CATHETER & ACCESSORY?
The FDA product code for TUBEGRIPPER, UROLOGICAL CATHETER & ACCESSORY is KOD.
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 Cathaid, 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: KOD)
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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