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FDA 510(k)

IRRIGATION CATHETER 4, 6 AND 10 FRENCH

K-Number: K902256 · 1991-02-15

Decision Date1991-02-15
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

IRRIGATION CATHETER 4, 6 AND 10 FRENCH is the device name listed in this FDA 510(k) record. The listed applicant is Applied Vascular Devices, Inc.. It received FDA 510(k) clearance on 1991-02-15 under 510(k) number K902256. 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 IRRIGATION CATHETER 4, 6 AND 10 FRENCH?

IRRIGATION CATHETER 4, 6 AND 10 FRENCH is a medical device that received FDA 510(k) clearance on 1991-02-15. The listed applicant is Applied Vascular Devices, Inc.. The 510(k) number is K902256.

When did IRRIGATION CATHETER 4, 6 AND 10 FRENCH receive FDA 510(k) clearance?

IRRIGATION CATHETER 4, 6 AND 10 FRENCH received FDA 510(k) clearance on 1991-02-15, under 510(k) number K902256.

Who is the listed applicant for IRRIGATION CATHETER 4, 6 AND 10 FRENCH?

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

What is the FDA product code for IRRIGATION CATHETER 4, 6 AND 10 FRENCH?

The FDA product code for IRRIGATION CATHETER 4, 6 AND 10 FRENCH is DQY.

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 Applied Vascular Devices, 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.

View all 21 devices →

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.

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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