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FDA 510(k)

TUBEGRIPPER, UROLOGICAL CATHETER & ACCESSORY

K-Number: K863958 · 1986-11-04

ApplicantCathaid, Inc.
Decision Date1986-11-04
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TUBEGRIPPER, UROLOGICAL CATHETER & ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Cathaid, Inc.. It received FDA 510(k) clearance on 1986-11-04 under 510(k) number K863958. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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