Mission Urinalysis Reagent Strips (Microalbumin/Creatinine)

FDA 510(k) K150330 · ACON Laboratories, Inc.

Substantially Equivalent

510(k) numberK150330

Submission

Device name
Mission Urinalysis Reagent Strips (Microalbumin/Creatinine)
Applicant
ACON Laboratories, Inc.
San Diego, CA, US
Received
February 10, 2015
Decision date
April 30, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JIR – Indicator Method, Protein Or Albumin (Urinary, Non-Quant.)
Device class
Class I (low risk)
Regulation
21 CFR 862.1645
Specialty
Clinical Chemistry

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Questions and answers

When was Mission Urinalysis Reagent Strips (Microalbumin/Creatinine) cleared by the FDA?

Mission Urinalysis Reagent Strips (Microalbumin/Creatinine) (K150330) received a 510(k) decision of Substantially Equivalent on April 30, 2015, 79 days after the submission was received.

What is the product code of K150330?

The FDA product code is JIR – Indicator Method, Protein Or Albumin (Urinary, Non-Quant.), a Class I (low risk) device regulated under 21 CFR 862.1645.