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FDA 510(k)

ANESTY 10

K-Number: K880744 · 1989-02-09

ApplicantNihon Medix Co., Ltd.
Decision Date1989-02-09
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ANESTY 10 is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Medix Co., Ltd.. It received FDA 510(k) clearance on 1989-02-09 under 510(k) number K880744. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANESTY 10?

ANESTY 10 is a medical device that received FDA 510(k) clearance on 1989-02-09. The listed applicant is Nihon Medix Co., Ltd.. The 510(k) number is K880744.

When did ANESTY 10 receive FDA 510(k) clearance?

ANESTY 10 received FDA 510(k) clearance on 1989-02-09, under 510(k) number K880744.

Who is the listed applicant for ANESTY 10?

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

What is the FDA product code for ANESTY 10?

The FDA product code for ANESTY 10 is GZJ.

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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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