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FDA 510(k)

CHALLENGE 3000 NEUROLOGICAL BOOSTER

K-Number: K903148 · 1991-12-10

ApplicantMaximum Performance Technologies, Mpts, Inc.
Decision Date1991-12-10
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CHALLENGE 3000 NEUROLOGICAL BOOSTER is the device name listed in this FDA 510(k) record. The listed applicant is Maximum Performance Technologies, Mpts, Inc.. It received FDA 510(k) clearance on 1991-12-10 under 510(k) number K903148. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHALLENGE 3000 NEUROLOGICAL BOOSTER?

CHALLENGE 3000 NEUROLOGICAL BOOSTER is a medical device that received FDA 510(k) clearance on 1991-12-10. The listed applicant is Maximum Performance Technologies, Mpts, Inc.. The 510(k) number is K903148.

When did CHALLENGE 3000 NEUROLOGICAL BOOSTER receive FDA 510(k) clearance?

CHALLENGE 3000 NEUROLOGICAL BOOSTER received FDA 510(k) clearance on 1991-12-10, under 510(k) number K903148.

Who is the listed applicant for CHALLENGE 3000 NEUROLOGICAL BOOSTER?

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

What is the FDA product code for CHALLENGE 3000 NEUROLOGICAL BOOSTER?

The FDA product code for CHALLENGE 3000 NEUROLOGICAL BOOSTER is IPF.

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Other records listing Maximum Performance Technologies, Mpts, Inc. as applicant

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Related Devices (Code: IPF)

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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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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