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FDA 510(k)

TERUMO GAS FILTER

K-Number: K021020 · 2002-06-10

ApplicantTerumo Cardiovascular Systems Corp.
Decision Date2002-06-10
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TERUMO GAS FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Cardiovascular Systems Corp.. It received FDA 510(k) clearance on 2002-06-10 under 510(k) number K021020. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TERUMO GAS FILTER?

TERUMO GAS FILTER is a medical device that received FDA 510(k) clearance on 2002-06-10. The listed applicant is Terumo Cardiovascular Systems Corp.. The 510(k) number is K021020.

When did TERUMO GAS FILTER receive FDA 510(k) clearance?

TERUMO GAS FILTER received FDA 510(k) clearance on 2002-06-10, under 510(k) number K021020.

Who is the listed applicant for TERUMO GAS FILTER?

The FDA 510(k) record lists Terumo Cardiovascular Systems Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TERUMO GAS FILTER?

The FDA product code for TERUMO GAS FILTER is CAH.

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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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