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FDA 510(k)

WIRECLIP TORQUER

K-Number: K003398 · 2000-12-01

ApplicantBoston Scientific Corporation Northwest Technology
Decision Date2000-12-01
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WIRECLIP TORQUER is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corporation Northwest Technology. It received FDA 510(k) clearance on 2000-12-01 under 510(k) number K003398. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WIRECLIP TORQUER?

WIRECLIP TORQUER is a medical device that received FDA 510(k) clearance on 2000-12-01. The listed applicant is Boston Scientific Corporation Northwest Technology. The 510(k) number is K003398.

When did WIRECLIP TORQUER receive FDA 510(k) clearance?

WIRECLIP TORQUER received FDA 510(k) clearance on 2000-12-01, under 510(k) number K003398.

Who is the listed applicant for WIRECLIP TORQUER?

The FDA 510(k) record lists Boston Scientific Corporation Northwest Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WIRECLIP TORQUER?

The FDA product code for WIRECLIP TORQUER is DQX.

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Other records listing Boston Scientific Corporation Northwest Technology as applicant

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Related Devices (Code: DQX)

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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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