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FDA 510(k)

WILLIAM HARVEY H-4700 FILTER/CARDIO

K-Number: K841079 · 1984-04-17

ApplicantC.R. Bard, Inc.
Decision Date1984-04-17
Product CodeDTN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WILLIAM HARVEY H-4700 FILTER/CARDIO 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 1984-04-17 under 510(k) number K841079. 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-4700 FILTER/CARDIO?

WILLIAM HARVEY H-4700 FILTER/CARDIO is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K841079.

When did WILLIAM HARVEY H-4700 FILTER/CARDIO receive FDA 510(k) clearance?

WILLIAM HARVEY H-4700 FILTER/CARDIO received FDA 510(k) clearance on 1984-04-17, under 510(k) number K841079.

Who is the listed applicant for WILLIAM HARVEY H-4700 FILTER/CARDIO?

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-4700 FILTER/CARDIO?

The FDA product code for WILLIAM HARVEY H-4700 FILTER/CARDIO 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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