510(k) K932161

UREA NITROGEN TEST ITEM NUMBER 65408 by Em Diagnostic Systems, Inc. — Product Code CDQ

K932161 is an FDA 510(k) premarket notification submitted by Em Diagnostic Systems, Inc. for the device "UREA NITROGEN TEST ITEM NUMBER 65408". The FDA issued a decision of Substantially Equivalent on September 8, 1993. The device falls under product code CDQ (Urease And Glutamic Dehydrogenase, Urea Nitrogen), a Class II device regulated under 21 CFR 862.1770. Em Diagnostic Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 8, 1993
Date Received
May 4, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Urease And Glutamic Dehydrogenase, Urea Nitrogen
Device Class
Class II
Regulation Number
862.1770
Review Panel
CH
Submission Type