AUTOMATED URINALYSIS SYSTEM— 510(k) K813056

Substantially Equivalent

Kyoto Daiichi Kagaku Co., Ltd.

FDA 510(k) clearance K813056 for AUTOMATED URINALYSIS SYSTEM, Substantially Equivalent on 1982-05-05. Applicant: Kyoto Daiichi Kagaku Co., Ltd.. Device class: 1.

Clearance details

Applicant
Kyoto Daiichi Kagaku Co., Ltd.
Product code
Code KQO
Device class
Class 1
Regulation
21 CFR 862.2900
Advisory panel
Clinical Chemistry
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Walker, MI, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code KQO

view all

More clearances from Kyoto Daiichi Kagaku Co., Ltd.

view all

Data sourced from openFDA. This site is unofficial and independent of the FDA.