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FDA 510(k)

BARD WILLIAM HARVEY CARDIOTOMY RESERVOIR

K-Number: K862920 · 1986-09-29

ApplicantC.R. Bard, Inc.
Decision Date1986-09-29
Product CodeDTN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BARD WILLIAM HARVEY CARDIOTOMY RESERVOIR 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 1986-09-29 under 510(k) number K862920. 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 BARD WILLIAM HARVEY CARDIOTOMY RESERVOIR?

BARD WILLIAM HARVEY CARDIOTOMY RESERVOIR is a medical device that received FDA 510(k) clearance on 1986-09-29. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K862920.

When did BARD WILLIAM HARVEY CARDIOTOMY RESERVOIR receive FDA 510(k) clearance?

BARD WILLIAM HARVEY CARDIOTOMY RESERVOIR received FDA 510(k) clearance on 1986-09-29, under 510(k) number K862920.

Who is the listed applicant for BARD WILLIAM HARVEY CARDIOTOMY RESERVOIR?

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 WILLIAM HARVEY CARDIOTOMY RESERVOIR?

The FDA product code for BARD WILLIAM HARVEY CARDIOTOMY RESERVOIR is DTN.

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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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