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FDA 510(k)

GLUCOMETER QC BLOOD METER, AMES GLUCO SYSTEM PRINT

K-Number: K871835 · 1987-12-22

ApplicantMiles Laboratories, Inc.
Decision Date1987-12-22
Product CodeCGA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GLUCOMETER QC BLOOD METER, AMES GLUCO SYSTEM PRINT is the device name listed in this FDA 510(k) record. The listed applicant is Miles Laboratories, Inc.. It received FDA 510(k) clearance on 1987-12-22 under 510(k) number K871835. 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 GLUCOMETER QC BLOOD METER, AMES GLUCO SYSTEM PRINT?

GLUCOMETER QC BLOOD METER, AMES GLUCO SYSTEM PRINT is a medical device that received FDA 510(k) clearance on 1987-12-22. The listed applicant is Miles Laboratories, Inc.. The 510(k) number is K871835.

When did GLUCOMETER QC BLOOD METER, AMES GLUCO SYSTEM PRINT receive FDA 510(k) clearance?

GLUCOMETER QC BLOOD METER, AMES GLUCO SYSTEM PRINT received FDA 510(k) clearance on 1987-12-22, under 510(k) number K871835.

Who is the listed applicant for GLUCOMETER QC BLOOD METER, AMES GLUCO SYSTEM PRINT?

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

What is the FDA product code for GLUCOMETER QC BLOOD METER, AMES GLUCO SYSTEM PRINT?

The FDA product code for GLUCOMETER QC BLOOD METER, AMES GLUCO SYSTEM PRINT is CGA.

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Other records listing Miles Laboratories, Inc. 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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