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FDA 510(k)

USCI DOPPLER CATHETER SYSTEM

K-Number: K810414 · 1981-08-12

ApplicantC.R. Bard, Inc.
Decision Date1981-08-12
Product CodeJOP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

USCI DOPPLER CATHETER SYSTEM 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 1981-08-12 under 510(k) number K810414. The device is classified under product code JOP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the USCI DOPPLER CATHETER SYSTEM?

USCI DOPPLER CATHETER SYSTEM is a medical device that received FDA 510(k) clearance on 1981-08-12. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K810414.

When did USCI DOPPLER CATHETER SYSTEM receive FDA 510(k) clearance?

USCI DOPPLER CATHETER SYSTEM received FDA 510(k) clearance on 1981-08-12, under 510(k) number K810414.

Who is the listed applicant for USCI DOPPLER CATHETER SYSTEM?

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 DOPPLER CATHETER SYSTEM?

The FDA product code for USCI DOPPLER CATHETER SYSTEM is JOP.

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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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