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FDA 510(k)

GLUCOSE TOLERANCE BEVERAGE

K-Number: K042183 · 2004-10-27

ApplicantEver Scientific
Decision Date2004-10-27
Product CodeMRV
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GLUCOSE TOLERANCE BEVERAGE is the device name listed in this FDA 510(k) record. The listed applicant is Ever Scientific. It received FDA 510(k) clearance on 2004-10-27 under 510(k) number K042183. The device is classified under product code MRV. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLUCOSE TOLERANCE BEVERAGE?

GLUCOSE TOLERANCE BEVERAGE is a medical device that received FDA 510(k) clearance on 2004-10-27. The listed applicant is Ever Scientific. The 510(k) number is K042183.

When did GLUCOSE TOLERANCE BEVERAGE receive FDA 510(k) clearance?

GLUCOSE TOLERANCE BEVERAGE received FDA 510(k) clearance on 2004-10-27, under 510(k) number K042183.

Who is the listed applicant for GLUCOSE TOLERANCE BEVERAGE?

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

What is the FDA product code for GLUCOSE TOLERANCE BEVERAGE?

The FDA product code for GLUCOSE TOLERANCE BEVERAGE is MRV.

Related Clinical Trials

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Related Devices (Code: MRV)

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.

K120247EASYDEXVineland Syrup, Inc.K032753GLUCOSE TOLERANCE BEVERAGEPerk Scientific, Inc.

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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