510(k) K960054

900UDX URINE PATHOLOGY SYSTEM by Intl. Remote Imaging Systems — Product Code KQO

K960054 is an FDA 510(k) premarket notification submitted by Intl. Remote Imaging Systems for the device "900UDX URINE PATHOLOGY SYSTEM". The FDA issued a decision of Substantially Equivalent on March 22, 1996. 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
March 22, 1996
Date Received
January 4, 1996
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