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FDA 510(k)

JOGUIDE CARDIOVASCULAR GUIDING C ATHETER

K-Number: K021088 · 2002-05-02

ApplicantJomed Catheter, Inc.
Decision Date2002-05-02
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

JOGUIDE CARDIOVASCULAR GUIDING C ATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Jomed Catheter, Inc.. It received FDA 510(k) clearance on 2002-05-02 under 510(k) number K021088. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOGUIDE CARDIOVASCULAR GUIDING C ATHETER?

JOGUIDE CARDIOVASCULAR GUIDING C ATHETER is a medical device that received FDA 510(k) clearance on 2002-05-02. The listed applicant is Jomed Catheter, Inc.. The 510(k) number is K021088.

When did JOGUIDE CARDIOVASCULAR GUIDING C ATHETER receive FDA 510(k) clearance?

JOGUIDE CARDIOVASCULAR GUIDING C ATHETER received FDA 510(k) clearance on 2002-05-02, under 510(k) number K021088.

Who is the listed applicant for JOGUIDE CARDIOVASCULAR GUIDING C ATHETER?

The FDA 510(k) record lists Jomed Catheter, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JOGUIDE CARDIOVASCULAR GUIDING C ATHETER?

The FDA product code for JOGUIDE CARDIOVASCULAR GUIDING C ATHETER is DQY.

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Related Devices (Code: DQY)

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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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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