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FDA 510(k)

USCI UNCOATED GUIDING CATHETERS

K-Number: K894682 · 1989-09-12

ApplicantC.R. Bard, Inc.
Decision Date1989-09-12
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

USCI UNCOATED GUIDING CATHETERS 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 1989-09-12 under 510(k) number K894682. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the USCI UNCOATED GUIDING CATHETERS?

USCI UNCOATED GUIDING CATHETERS is a medical device that received FDA 510(k) clearance on 1989-09-12. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K894682.

When did USCI UNCOATED GUIDING CATHETERS receive FDA 510(k) clearance?

USCI UNCOATED GUIDING CATHETERS received FDA 510(k) clearance on 1989-09-12, under 510(k) number K894682.

Who is the listed applicant for USCI UNCOATED GUIDING CATHETERS?

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 UNCOATED GUIDING CATHETERS?

The FDA product code for USCI UNCOATED GUIDING CATHETERS is DQY.

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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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