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FDA 510(k)

BARD CRITICAL CARE THERMODILUTIN CATHETER W/INFUSI

K-Number: K850952 · 1985-08-05

ApplicantC.R. Bard, Inc.
Decision Date1985-08-05
Product CodeDYG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BARD CRITICAL CARE THERMODILUTIN CATHETER W/INFUSI 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 1985-08-05 under 510(k) number K850952. The device is classified under product code DYG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD CRITICAL CARE THERMODILUTIN CATHETER W/INFUSI?

BARD CRITICAL CARE THERMODILUTIN CATHETER W/INFUSI is a medical device that received FDA 510(k) clearance on 1985-08-05. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K850952.

When did BARD CRITICAL CARE THERMODILUTIN CATHETER W/INFUSI receive FDA 510(k) clearance?

BARD CRITICAL CARE THERMODILUTIN CATHETER W/INFUSI received FDA 510(k) clearance on 1985-08-05, under 510(k) number K850952.

Who is the listed applicant for BARD CRITICAL CARE THERMODILUTIN CATHETER W/INFUSI?

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 BARD CRITICAL CARE THERMODILUTIN CATHETER W/INFUSI?

The FDA product code for BARD CRITICAL CARE THERMODILUTIN CATHETER W/INFUSI is DYG.

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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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