FDA 510(k)

USCI MACH 10 GUIDE WIRE WITH PRO/PEL COATING

K-Number: K933466 · 1993-10-01

Decision Date1993-10-01

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

USCI MACH 10 GUIDE WIRE WITH PRO/PEL COATING is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1993-10-01 under 510(k) number K933466. 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 USCI MACH 10 GUIDE WIRE WITH PRO/PEL COATING?

USCI MACH 10 GUIDE WIRE WITH PRO/PEL COATING is a medical device that received FDA 510(k) clearance on 1993-10-01. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K933466.

When did USCI MACH 10 GUIDE WIRE WITH PRO/PEL COATING receive FDA 510(k) clearance?

USCI MACH 10 GUIDE WIRE WITH PRO/PEL COATING received FDA 510(k) clearance on 1993-10-01, under 510(k) number K933466.

Who is the listed applicant for USCI MACH 10 GUIDE WIRE WITH PRO/PEL COATING?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for USCI MACH 10 GUIDE WIRE WITH PRO/PEL COATING?

The FDA product code for USCI MACH 10 GUIDE WIRE WITH PRO/PEL COATING is 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.