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FDA 510(k)

STRIDE MICROCATHETER

K-Number: K062885 · 2007-06-13

ApplicantAsahi Intecc Co., Ltd.
Decision Date2007-06-13
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STRIDE MICROCATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Asahi Intecc Co., Ltd.. It received FDA 510(k) clearance on 2007-06-13 under 510(k) number K062885. 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 STRIDE MICROCATHETER?

STRIDE MICROCATHETER is a medical device that received FDA 510(k) clearance on 2007-06-13. The listed applicant is Asahi Intecc Co., Ltd.. The 510(k) number is K062885.

When did STRIDE MICROCATHETER receive FDA 510(k) clearance?

STRIDE MICROCATHETER received FDA 510(k) clearance on 2007-06-13, under 510(k) number K062885.

Who is the listed applicant for STRIDE MICROCATHETER?

The FDA 510(k) record lists Asahi Intecc Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STRIDE MICROCATHETER?

The FDA product code for STRIDE MICROCATHETER is DQY.

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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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