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FDA 510(k)

ZIVF-AIRE

K-Number: K041952 · 2005-09-08

ApplicantZander Medical Supplies, Inc.
Decision Date2005-09-08
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ZIVF-AIRE is the device name listed in this FDA 510(k) record. The listed applicant is Zander Medical Supplies, Inc.. It received FDA 510(k) clearance on 2005-09-08 under 510(k) number K041952. The device is classified under product code MQG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZIVF-AIRE?

ZIVF-AIRE is a medical device that received FDA 510(k) clearance on 2005-09-08. The listed applicant is Zander Medical Supplies, Inc.. The 510(k) number is K041952.

When did ZIVF-AIRE receive FDA 510(k) clearance?

ZIVF-AIRE received FDA 510(k) clearance on 2005-09-08, under 510(k) number K041952.

Who is the listed applicant for ZIVF-AIRE?

The FDA 510(k) record lists Zander Medical Supplies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ZIVF-AIRE?

The FDA product code for ZIVF-AIRE is MQG.

Other records listing Zander Medical Supplies, Inc. as applicant

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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.

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