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FDA 510(k)

DISPO. AES.

K-Number: K821671 · 1982-07-28

ApplicantHiraoka New York, Inc.
Decision Date1982-07-28
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPO. AES. is the device name listed in this FDA 510(k) record. The listed applicant is Hiraoka New York, Inc.. It received FDA 510(k) clearance on 1982-07-28 under 510(k) number K821671. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPO. AES.?

DISPO. AES. is a medical device that received FDA 510(k) clearance on 1982-07-28. The listed applicant is Hiraoka New York, Inc.. The 510(k) number is K821671.

When did DISPO. AES. receive FDA 510(k) clearance?

DISPO. AES. received FDA 510(k) clearance on 1982-07-28, under 510(k) number K821671.

Who is the listed applicant for DISPO. AES.?

The FDA 510(k) record lists Hiraoka New York, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPO. AES.?

The FDA product code for DISPO. AES. is FMF.

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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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