Uriscan Optima II Urine Analyzer

FDA 510(k) K050801 · Yd Diagnostics

Substantially Equivalent

510(k) numberK050801

Submission

Device name
Uriscan Optima II Urine Analyzer
Applicant
Yd Diagnostics
La Canada, CA, US
Received
March 30, 2005
Decision date
April 20, 2005
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) statement available from FDA

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 Uriscan Optima II Urine Analyzer cleared by the FDA?

Uriscan Optima II Urine Analyzer (K050801) received a 510(k) decision of Substantially Equivalent on April 20, 2005, 21 days after the submission was received.

What is the product code of K050801?

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