FDA 510(k)

WILLIAM HARVEY OXYGENATING GAS FILTER

K-Number: K802906 · 1980-12-16

Decision Date1980-12-16

Product CodeKRI

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

WILLIAM HARVEY OXYGENATING GAS 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 1980-12-16 under 510(k) number K802906. The device is classified under product code KRI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILLIAM HARVEY OXYGENATING GAS FILTER?

WILLIAM HARVEY OXYGENATING GAS FILTER is a medical device that received FDA 510(k) clearance on 1980-12-16. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K802906.

When did WILLIAM HARVEY OXYGENATING GAS FILTER receive FDA 510(k) clearance?

WILLIAM HARVEY OXYGENATING GAS FILTER received FDA 510(k) clearance on 1980-12-16, under 510(k) number K802906.

Who is the listed applicant for WILLIAM HARVEY OXYGENATING GAS 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 OXYGENATING GAS FILTER?

The FDA product code for WILLIAM HARVEY OXYGENATING GAS FILTER is KRI.

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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.