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FDA 510(k)

AIR MEDICA III

K-Number: K920710 · 1992-05-04

ApplicantHinatawada Seimitsu Mfg. Co., Ltd.
Decision Date1992-05-04
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AIR MEDICA III is the device name listed in this FDA 510(k) record. The listed applicant is Hinatawada Seimitsu Mfg. Co., Ltd.. It received FDA 510(k) clearance on 1992-05-04 under 510(k) number K920710. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIR MEDICA III?

AIR MEDICA III is a medical device that received FDA 510(k) clearance on 1992-05-04. The listed applicant is Hinatawada Seimitsu Mfg. Co., Ltd.. The 510(k) number is K920710.

When did AIR MEDICA III receive FDA 510(k) clearance?

AIR MEDICA III received FDA 510(k) clearance on 1992-05-04, under 510(k) number K920710.

Who is the listed applicant for AIR MEDICA III?

The FDA 510(k) record lists Hinatawada Seimitsu Mfg. Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIR MEDICA III?

The FDA product code for AIR MEDICA III is EIA.

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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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