510(k) K952742

BLOOD UREA NITROGEN REAGENT SYSTEM by Medical Diagnostic Technologies, Inc. — Product Code CDQ

K952742 is an FDA 510(k) premarket notification submitted by Medical Diagnostic Technologies, Inc. for the device "BLOOD UREA NITROGEN REAGENT SYSTEM". The FDA issued a decision of Substantially Equivalent on August 11, 1995. The device falls under product code CDQ (Urease And Glutamic Dehydrogenase, Urea Nitrogen), a Class II device regulated under 21 CFR 862.1770. Medical Diagnostic Technologies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 11, 1995
Date Received
June 16, 1995
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