Biotel (Tm)/ Diabetes

FDA 510(k) K855239 · American Diagnostic Corp.

Substantially Equivalent

510(k) numberK855239

Submission

Device name
Biotel (Tm)/ Diabetes
Applicant
American Diagnostic Corp.
Wheaton, IL, US
Received
December 31, 1985
Decision date
June 13, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JIL – Method, Enzymatic, Glucose (Urinary, Non-Quantitative)
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1340
Specialty
Clinical Chemistry

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Questions and answers

When was Biotel (Tm)/ Diabetes cleared by the FDA?

Biotel (Tm)/ Diabetes (K855239) received a 510(k) decision of Substantially Equivalent on June 13, 1986, 164 days after the submission was received.

What is the product code of K855239?

The FDA product code is JIL – Method, Enzymatic, Glucose (Urinary, Non-Quantitative), a Class II (moderate risk) device regulated under 21 CFR 862.1340.