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FDA 510(k)

COAXIAL CATHETER SET

K-Number: K902694 · 1990-08-28

ApplicantCook Ob/Gyn
Decision Date1990-08-28
Product CodeHDR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

COAXIAL CATHETER SET is the device name listed in this FDA 510(k) record. The listed applicant is Cook Ob/Gyn. It received FDA 510(k) clearance on 1990-08-28 under 510(k) number K902694. The device is classified under product code HDR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COAXIAL CATHETER SET?

COAXIAL CATHETER SET is a medical device that received FDA 510(k) clearance on 1990-08-28. The listed applicant is Cook Ob/Gyn. The 510(k) number is K902694.

When did COAXIAL CATHETER SET receive FDA 510(k) clearance?

COAXIAL CATHETER SET received FDA 510(k) clearance on 1990-08-28, under 510(k) number K902694.

Who is the listed applicant for COAXIAL CATHETER SET?

The FDA 510(k) record lists Cook Ob/Gyn as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COAXIAL CATHETER SET?

The FDA product code for COAXIAL CATHETER SET is HDR.

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Other records listing Cook Ob/Gyn 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.

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Related Devices (Code: HDR)

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.

K242031Béa Applicator (BAP-GB-01)Stepone Fertility Ltd (T/A Béa Fertility)K222969FERTI-LILY Conception CupRosesta Medical BVK993953OVES CERVICAL CAPVeos , Ltd.K945131IMAGYN INTRAUTERINE INSEMINATION DEVICEImagyn Medical, Inc.K950714COOK INSEMINATION CUPCook Urological, Inc.K902171MINISPACE(TM) IUI CATHETERPharmacia, Inc.

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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