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FDA 510(k)

USCI PRO FLO XT,SOFT TIP, AND XT SOFT TIP ANGIOGRAPHIC

K-Number: K960056 · 1996-10-23

ApplicantC.R. Bard, Inc.
Decision Date1996-10-23
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

USCI PRO FLO XT,SOFT TIP, AND XT SOFT TIP ANGIOGRAPHIC 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 1996-10-23 under 510(k) number K960056. 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 PRO FLO XT,SOFT TIP, AND XT SOFT TIP ANGIOGRAPHIC?

USCI PRO FLO XT,SOFT TIP, AND XT SOFT TIP ANGIOGRAPHIC is a medical device that received FDA 510(k) clearance on 1996-10-23. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K960056.

When did USCI PRO FLO XT,SOFT TIP, AND XT SOFT TIP ANGIOGRAPHIC receive FDA 510(k) clearance?

USCI PRO FLO XT,SOFT TIP, AND XT SOFT TIP ANGIOGRAPHIC received FDA 510(k) clearance on 1996-10-23, under 510(k) number K960056.

Who is the listed applicant for USCI PRO FLO XT,SOFT TIP, AND XT SOFT TIP ANGIOGRAPHIC?

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 PRO FLO XT,SOFT TIP, AND XT SOFT TIP ANGIOGRAPHIC?

The FDA product code for USCI PRO FLO XT,SOFT TIP, AND XT SOFT TIP ANGIOGRAPHIC 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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