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FDA 510(k)

TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR SU

K-Number: K864115 · 1986-11-07

ApplicantCathaid, Inc.
Decision Date1986-11-07
Product CodeKGZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR SU is the device name listed in this FDA 510(k) record. The listed applicant is Cathaid, Inc.. It received FDA 510(k) clearance on 1986-11-07 under 510(k) number K864115. The device is classified under product code KGZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR SU?

TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR SU is a medical device that received FDA 510(k) clearance on 1986-11-07. The listed applicant is Cathaid, Inc.. The 510(k) number is K864115.

When did TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR SU receive FDA 510(k) clearance?

TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR SU received FDA 510(k) clearance on 1986-11-07, under 510(k) number K864115.

Who is the listed applicant for TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR SU?

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, DRAINAGE CATHETER & ACCESSORY FOR SU?

The FDA product code for TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR SU is KGZ.

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: KGZ)

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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