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FDA 510(k)

USCI SATIN FINISH SOFT TIP ANGIOGRAPHIC CATHETER

K-Number: K905727 · 1991-02-01

ApplicantC.R. Bard, Inc.
Decision Date1991-02-01
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

USCI SATIN FINISH SOFT TIP ANGIOGRAPHIC CATHETER 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 1991-02-01 under 510(k) number K905727. 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 SATIN FINISH SOFT TIP ANGIOGRAPHIC CATHETER?

USCI SATIN FINISH SOFT TIP ANGIOGRAPHIC CATHETER is a medical device that received FDA 510(k) clearance on 1991-02-01. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K905727.

When did USCI SATIN FINISH SOFT TIP ANGIOGRAPHIC CATHETER receive FDA 510(k) clearance?

USCI SATIN FINISH SOFT TIP ANGIOGRAPHIC CATHETER received FDA 510(k) clearance on 1991-02-01, under 510(k) number K905727.

Who is the listed applicant for USCI SATIN FINISH SOFT TIP ANGIOGRAPHIC CATHETER?

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 SATIN FINISH SOFT TIP ANGIOGRAPHIC CATHETER?

The FDA product code for USCI SATIN FINISH SOFT TIP ANGIOGRAPHIC CATHETER 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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