510(k) K972141

THE YELLOW IRIS URINALYSIS WORKSTATION by Intl. Remote Imaging Systems — Product Code KQO

K972141 is an FDA 510(k) premarket notification submitted by Intl. Remote Imaging Systems for the device "THE YELLOW IRIS URINALYSIS WORKSTATION". The FDA issued a decision of Substantially Equivalent on August 25, 1997. The device falls under product code KQO (Automated Urinalysis System), a Class I device regulated under 21 CFR 862.2900. Intl. Remote Imaging Systems has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 25, 1997
Date Received
June 6, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Automated Urinalysis System
Device Class
Class I
Regulation Number
862.2900
Review Panel
CH
Submission Type