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FDA 510(k)

USCI LINX EZ GUIDE WIRE EXTEN. W/ PRO/PEL COATING

K-Number: K922105 · 1992-11-17

ApplicantC.R. Bard, Inc.
Decision Date1992-11-17
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

USCI LINX EZ GUIDE WIRE EXTEN. W/ 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 1992-11-17 under 510(k) number K922105. 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 USCI LINX EZ GUIDE WIRE EXTEN. W/ PRO/PEL COATING?

USCI LINX EZ GUIDE WIRE EXTEN. W/ PRO/PEL COATING is a medical device that received FDA 510(k) clearance on 1992-11-17. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K922105.

When did USCI LINX EZ GUIDE WIRE EXTEN. W/ PRO/PEL COATING receive FDA 510(k) clearance?

USCI LINX EZ GUIDE WIRE EXTEN. W/ PRO/PEL COATING received FDA 510(k) clearance on 1992-11-17, under 510(k) number K922105.

Who is the listed applicant for USCI LINX EZ GUIDE WIRE EXTEN. W/ 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 LINX EZ GUIDE WIRE EXTEN. W/ PRO/PEL COATING?

The FDA product code for USCI LINX EZ GUIDE WIRE EXTEN. W/ PRO/PEL COATING is 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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