510(k) K903335

SYSTEMATE URIC ACID (URCA) ITEM NUMBER 65422 by Em Diagnostic Systems, Inc. — Product Code CDO

K903335 is an FDA 510(k) premarket notification submitted by Em Diagnostic Systems, Inc. for the device "SYSTEMATE URIC ACID (URCA) ITEM NUMBER 65422". The FDA issued a decision of Substantially Equivalent on August 17, 1990. The device falls under product code CDO (Acid, Uric, Uricase (U.V.)), a Class I device regulated under 21 CFR 862.1775. Em Diagnostic Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 17, 1990
Date Received
July 25, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Acid, Uric, Uricase (U.V.)
Device Class
Class I
Regulation Number
862.1775
Review Panel
CH
Submission Type