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FDA 510(k)

0.035 IN. WISE WIRE

K-Number: K942927 · 1995-06-13

ApplicantBoston Scientific Corp
Decision Date1995-06-13
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

0.035 IN. WISE WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 1995-06-13 under 510(k) number K942927. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 0.035 IN. WISE WIRE?

0.035 IN. WISE WIRE is a medical device that received FDA 510(k) clearance on 1995-06-13. The listed applicant is Boston Scientific Corp. The 510(k) number is K942927.

When did 0.035 IN. WISE WIRE receive FDA 510(k) clearance?

0.035 IN. WISE WIRE received FDA 510(k) clearance on 1995-06-13, under 510(k) number K942927.

Who is the listed applicant for 0.035 IN. WISE WIRE?

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

What is the FDA product code for 0.035 IN. WISE WIRE?

The FDA product code for 0.035 IN. WISE WIRE is DQO.

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Related Devices (Code: DQO)

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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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