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FDA 510(k)

MEDISON 1500

K-Number: K924432 · 1993-11-24

ApplicantMedison Co., Ltd.
Decision Date1993-11-24
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDISON 1500 is the device name listed in this FDA 510(k) record. The listed applicant is Medison Co., Ltd.. It received FDA 510(k) clearance on 1993-11-24 under 510(k) number K924432. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDISON 1500?

MEDISON 1500 is a medical device that received FDA 510(k) clearance on 1993-11-24. The listed applicant is Medison Co., Ltd.. The 510(k) number is K924432.

When did MEDISON 1500 receive FDA 510(k) clearance?

MEDISON 1500 received FDA 510(k) clearance on 1993-11-24, under 510(k) number K924432.

Who is the listed applicant for MEDISON 1500?

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

What is the FDA product code for MEDISON 1500?

The FDA product code for MEDISON 1500 is IYO.

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Other records listing Medison Co., Ltd. as applicant

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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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