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FDA 510(k)

KINETIC DETERMINATION OF UV GLUCOSE

K-Number: K791110 · 1979-08-03

ApplicantThe Dow Chemical Co.
Decision Date1979-08-03
Product CodeLFR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KINETIC DETERMINATION OF UV GLUCOSE is the device name listed in this FDA 510(k) record. The listed applicant is The Dow Chemical Co.. It received FDA 510(k) clearance on 1979-08-03 under 510(k) number K791110. The device is classified under product code LFR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KINETIC DETERMINATION OF UV GLUCOSE?

KINETIC DETERMINATION OF UV GLUCOSE is a medical device that received FDA 510(k) clearance on 1979-08-03. The listed applicant is The Dow Chemical Co.. The 510(k) number is K791110.

When did KINETIC DETERMINATION OF UV GLUCOSE receive FDA 510(k) clearance?

KINETIC DETERMINATION OF UV GLUCOSE received FDA 510(k) clearance on 1979-08-03, under 510(k) number K791110.

Who is the listed applicant for KINETIC DETERMINATION OF UV GLUCOSE?

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

What is the FDA product code for KINETIC DETERMINATION OF UV GLUCOSE?

The FDA product code for KINETIC DETERMINATION OF UV GLUCOSE is LFR.

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Other records listing The Dow Chemical Co. 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.

K823474ENZYMATIC GLUCOSE DETERMINATIONK822154UREA NITROGEN (ENZYMATIC) DETERMINATIONK821536DOWFLOW ALT-UV DETERMINATIONK821315DOWFLOW ENZYMATIC TRIGLYCERIDES DETERMK820675BILIRUBIN(TOTAL) DETERMINATION CTMSK820714DOW BILIRUBIN(DIRECT) DETERMINATION

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Related Devices (Code: LFR)

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.

K131366ACCU-CHEK AVIVA EXPERT BLOOD GLUCOSE MONITORING SYSTEMRoche Diagnostics Operations, Inc.K122688NOVA MAX MINI BLOOD GLUCOSE AND B-KETONE MONITORNova Biomedical CorporationK121433GOODLIFE CS-200 (SINGLE PATIENT USE), CS-200 PROFESSIONAL (MULTIPLE PATIENT USE) BLOOD GLUCOSE MONITORING SYSTEMSHmd Biomedical, Inc.K122435NOVA ONE BLOOD GLUCOSE MONITORNova Biomedical CorporationK113314PRECICHEK NS-101 POCT PROFESSIONAL BLOOD GLUCOSE MONITORING SYSTEMHmd Biomedical, Inc.K121224GENESIS HEALTH TECHNOLOGIES BLOOD GLUCOSE MONITORING SYSTEMTaidoc Technology Corporation

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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