FDA 510(k)

BARD DESAI CATHETER ELECTRODE

K-Number: K873995 · 1988-01-07

Decision Date1988-01-07

Product CodeDRF

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

BARD DESAI CATHETER ELECTRODE 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 1988-01-07 under 510(k) number K873995. 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 DESAI CATHETER ELECTRODE?

BARD DESAI CATHETER ELECTRODE is a medical device that received FDA 510(k) clearance on 1988-01-07. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K873995.

When did BARD DESAI CATHETER ELECTRODE receive FDA 510(k) clearance?

BARD DESAI CATHETER ELECTRODE received FDA 510(k) clearance on 1988-01-07, under 510(k) number K873995.

Who is the listed applicant for BARD DESAI CATHETER ELECTRODE?

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 DESAI CATHETER ELECTRODE?

The FDA product code for BARD DESAI CATHETER ELECTRODE 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.