510(k) K954158

STC DIAGNOSTICS AUTO-LYTE PH ASSAY by Solarcare Technologies Corp,Inc. — Product Code KQO

K954158 is an FDA 510(k) premarket notification submitted by Solarcare Technologies Corp,Inc. for the device "STC DIAGNOSTICS AUTO-LYTE PH ASSAY". The FDA issued a decision of Substantially Equivalent on April 30, 1996. The device falls under product code KQO (Automated Urinalysis System), a Class I device regulated under 21 CFR 862.2900. Solarcare Technologies Corp,Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 30, 1996
Date Received
September 5, 1995
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