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FDA 510(k)

ZEBRA UROLOGICAL GUIDEWIRE

K-Number: K942205 · 1994-07-07

ApplicantBoston Scientific Corp
Decision Date1994-07-07
Product CodeKNY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ZEBRA UROLOGICAL GUIDEWIRE 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 1994-07-07 under 510(k) number K942205. The device is classified under product code KNY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZEBRA UROLOGICAL GUIDEWIRE?

ZEBRA UROLOGICAL GUIDEWIRE is a medical device that received FDA 510(k) clearance on 1994-07-07. The listed applicant is Boston Scientific Corp. The 510(k) number is K942205.

When did ZEBRA UROLOGICAL GUIDEWIRE receive FDA 510(k) clearance?

ZEBRA UROLOGICAL GUIDEWIRE received FDA 510(k) clearance on 1994-07-07, under 510(k) number K942205.

Who is the listed applicant for ZEBRA UROLOGICAL GUIDEWIRE?

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 ZEBRA UROLOGICAL GUIDEWIRE?

The FDA product code for ZEBRA UROLOGICAL GUIDEWIRE is KNY.

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Other records listing Boston Scientific Corp as applicant

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Related Devices (Code: KNY)

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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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