FDA 510(k)

MODIFIED EPICARDIAL ARRAY

K-Number: K902228 · 1990-07-06

Decision Date1990-07-06

Product CodeDRF

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MODIFIED EPICARDIAL 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 1990-07-06 under 510(k) number K902228. 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 MODIFIED EPICARDIAL ARRAY?

MODIFIED EPICARDIAL ARRAY is a medical device that received FDA 510(k) clearance on 1990-07-06. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K902228.

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

MODIFIED EPICARDIAL ARRAY received FDA 510(k) clearance on 1990-07-06, under 510(k) number K902228.

Who is the listed applicant for MODIFIED EPICARDIAL 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 MODIFIED EPICARDIAL ARRAY?

The FDA product code for MODIFIED EPICARDIAL ARRAY is DRF.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.