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FDA 510(k)

CHECKMATE PLUS BLOOD GLUCOSE METER, TEST STRIP,ETC

K-Number: K931188 · 1993-05-26

ApplicantCascade Medical, Inc.
Decision Date1993-05-26
Product CodeCGA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CHECKMATE PLUS BLOOD GLUCOSE METER, TEST STRIP,ETC is the device name listed in this FDA 510(k) record. The listed applicant is Cascade Medical, Inc.. It received FDA 510(k) clearance on 1993-05-26 under 510(k) number K931188. The device is classified under product code CGA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHECKMATE PLUS BLOOD GLUCOSE METER, TEST STRIP,ETC?

CHECKMATE PLUS BLOOD GLUCOSE METER, TEST STRIP,ETC is a medical device that received FDA 510(k) clearance on 1993-05-26. The listed applicant is Cascade Medical, Inc.. The 510(k) number is K931188.

When did CHECKMATE PLUS BLOOD GLUCOSE METER, TEST STRIP,ETC receive FDA 510(k) clearance?

CHECKMATE PLUS BLOOD GLUCOSE METER, TEST STRIP,ETC received FDA 510(k) clearance on 1993-05-26, under 510(k) number K931188.

Who is the listed applicant for CHECKMATE PLUS BLOOD GLUCOSE METER, TEST STRIP,ETC?

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

What is the FDA product code for CHECKMATE PLUS BLOOD GLUCOSE METER, TEST STRIP,ETC?

The FDA product code for CHECKMATE PLUS BLOOD GLUCOSE METER, TEST STRIP,ETC is CGA.

Related Clinical Trials

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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Other records listing Cascade Medical, 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.

K896144AUTOSCAN, AUTOSTRIP AND AUTOCONTROL

Related Devices (Code: CGA)

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.

K252488ABL90 FLEX PLUS SystemRadiometer Medicals ApsK210933YSI 2900C Biochemistry AnalyzerYsi, Inc.K220328EasyStat 300Medica CorporationK223179Cholestech LDX ™ SystemAlere San Diego, Inc.K223755i-STAT G cartridge with the i-STAT 1 SystemAbbott Point of Care, Inc.K223710i-STAT CG8+ cartridge with the i-STAT 1 SystemAbbott Point of Care, 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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