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FDA 510(k)

BARD EPICARDIAL ELECTRODE ARRAY

K-Number: K872231 · 1987-10-09

ApplicantC.R. Bard, Inc.
Decision Date1987-10-09
Product CodeDRF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BARD EPICARDIAL ELECTRODE ARRAY 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 1987-10-09 under 510(k) number K872231. The device is classified under product code DRF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD EPICARDIAL ELECTRODE ARRAY?

BARD EPICARDIAL ELECTRODE ARRAY is a medical device that received FDA 510(k) clearance on 1987-10-09. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K872231.

When did BARD EPICARDIAL ELECTRODE ARRAY receive FDA 510(k) clearance?

BARD EPICARDIAL ELECTRODE ARRAY received FDA 510(k) clearance on 1987-10-09, under 510(k) number K872231.

Who is the listed applicant for BARD EPICARDIAL ELECTRODE ARRAY?

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 EPICARDIAL ELECTRODE ARRAY?

The FDA product code for BARD EPICARDIAL ELECTRODE ARRAY is DRF.

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Related Devices (Code: DRF)

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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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