FDA 510(k)

WILLIAM HARVEY H-71-5-F CARDIOTOMY

K-Number: K833479 · 1983-12-16

Decision Date1983-12-16

Product CodeDTN

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

WILLIAM HARVEY H-71-5-F CARDIOTOMY 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 1983-12-16 under 510(k) number K833479. The device is classified under product code DTN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILLIAM HARVEY H-71-5-F CARDIOTOMY?

WILLIAM HARVEY H-71-5-F CARDIOTOMY is a medical device that received FDA 510(k) clearance on 1983-12-16. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K833479.

When did WILLIAM HARVEY H-71-5-F CARDIOTOMY receive FDA 510(k) clearance?

WILLIAM HARVEY H-71-5-F CARDIOTOMY received FDA 510(k) clearance on 1983-12-16, under 510(k) number K833479.

Who is the listed applicant for WILLIAM HARVEY H-71-5-F CARDIOTOMY?

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 WILLIAM HARVEY H-71-5-F CARDIOTOMY?

The FDA product code for WILLIAM HARVEY H-71-5-F CARDIOTOMY is DTN.

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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.