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FDA 510(k)

MULTI III, IV

K-Number: K955860 · 1996-03-22

ApplicantExcel Tech. , Ltd.
Decision Date1996-03-22
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent for Some Indications

Device Summary

MULTI III, IV 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 1996-03-22 under 510(k) number K955860. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the MULTI III, IV?

MULTI III, IV is a medical device that received FDA 510(k) clearance on 1996-03-22. The listed applicant is Excel Tech. , Ltd.. The 510(k) number is K955860.

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

MULTI III, IV received FDA 510(k) clearance on 1996-03-22, under 510(k) number K955860.

Who is the listed applicant for MULTI III, IV?

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, IV?

The FDA product code for MULTI III, IV is LIH.

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Other records listing Excel Tech. , 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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