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FDA 510(k)

MULTACHOICE INSTRUMENTS

K-Number: K991814 · 1999-06-23

ApplicantDexide, Inc.
Decision Date1999-06-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MULTACHOICE INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Dexide, Inc.. It received FDA 510(k) clearance on 1999-06-23 under 510(k) number K991814. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTACHOICE INSTRUMENTS?

MULTACHOICE INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1999-06-23. The listed applicant is Dexide, Inc.. The 510(k) number is K991814.

When did MULTACHOICE INSTRUMENTS receive FDA 510(k) clearance?

MULTACHOICE INSTRUMENTS received FDA 510(k) clearance on 1999-06-23, under 510(k) number K991814.

Who is the listed applicant for MULTACHOICE INSTRUMENTS?

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

What is the FDA product code for MULTACHOICE INSTRUMENTS?

The FDA product code for MULTACHOICE INSTRUMENTS is GEI.

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Other records listing Dexide, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: GEI)

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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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