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FDA 510(k)

MULTI III

K-Number: K921953 · 1992-08-26

ApplicantExcel Tech. , Ltd.
Decision Date1992-08-26
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MULTI III is the device name listed in this FDA 510(k) record. The listed applicant is Excel Tech. , Ltd.. It received FDA 510(k) clearance on 1992-08-26 under 510(k) number K921953. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI III?

MULTI III is a medical device that received FDA 510(k) clearance on 1992-08-26. The listed applicant is Excel Tech. , Ltd.. The 510(k) number is K921953.

When did MULTI III receive FDA 510(k) clearance?

MULTI III received FDA 510(k) clearance on 1992-08-26, under 510(k) number K921953.

Who is the listed applicant for MULTI III?

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

What is the FDA product code for MULTI III?

The FDA product code for MULTI III is LIH.

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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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