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FDA 510(k)

WILLIAM HARVEY H-625 ARTERIAL FILTER

K-Number: K820472 · 1982-03-15

ApplicantC.R. Bard, Inc.
Decision Date1982-03-15
Product CodeDTM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WILLIAM HARVEY H-625 ARTERIAL FILTER 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 1982-03-15 under 510(k) number K820472. The device is classified under product code DTM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILLIAM HARVEY H-625 ARTERIAL FILTER?

WILLIAM HARVEY H-625 ARTERIAL FILTER is a medical device that received FDA 510(k) clearance on 1982-03-15. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K820472.

When did WILLIAM HARVEY H-625 ARTERIAL FILTER receive FDA 510(k) clearance?

WILLIAM HARVEY H-625 ARTERIAL FILTER received FDA 510(k) clearance on 1982-03-15, under 510(k) number K820472.

Who is the listed applicant for WILLIAM HARVEY H-625 ARTERIAL FILTER?

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-625 ARTERIAL FILTER?

The FDA product code for WILLIAM HARVEY H-625 ARTERIAL FILTER is DTM.

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Related Devices (Code: DTM)

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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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