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FDA 510(k)

DIASCAN* BLOOD GLUCOSE SELF-MONITORING TEST STRIPS

K-Number: K872505 · 1987-10-20

ApplicantHome Diagnostics, Inc.
Decision Date1987-10-20
Product CodeCGA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIASCAN* BLOOD GLUCOSE SELF-MONITORING TEST STRIPS is the device name listed in this FDA 510(k) record. The listed applicant is Home Diagnostics, Inc.. It received FDA 510(k) clearance on 1987-10-20 under 510(k) number K872505. 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 DIASCAN* BLOOD GLUCOSE SELF-MONITORING TEST STRIPS?

DIASCAN* BLOOD GLUCOSE SELF-MONITORING TEST STRIPS is a medical device that received FDA 510(k) clearance on 1987-10-20. The listed applicant is Home Diagnostics, Inc.. The 510(k) number is K872505.

When did DIASCAN* BLOOD GLUCOSE SELF-MONITORING TEST STRIPS receive FDA 510(k) clearance?

DIASCAN* BLOOD GLUCOSE SELF-MONITORING TEST STRIPS received FDA 510(k) clearance on 1987-10-20, under 510(k) number K872505.

Who is the listed applicant for DIASCAN* BLOOD GLUCOSE SELF-MONITORING TEST STRIPS?

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

What is the FDA product code for DIASCAN* BLOOD GLUCOSE SELF-MONITORING TEST STRIPS?

The FDA product code for DIASCAN* BLOOD GLUCOSE SELF-MONITORING TEST STRIPS is CGA.

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Other records listing Home Diagnostics, 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.

K090495TRUEBALANCE BLOOD GLUCOSE SYSTEMK080641TRUERESULT BLOOD GLUCOSE SYSTEM E4H01-81K080710TRUE2GO BLOOD GLUCOSE SYSTEM, MODEL F4H01-81K070593TRACKRECORD DATA MANAGEMENT SOFTWAREK060793ELEMENT BLOOD GLUCOSE TEST SYSTEMK051147SIDEKICK BLOOD GLUCOSE TEST SYSTEM

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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.

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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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