510(k) K952746

ALKALINE PHOSPHATASE REAGENT SYSTEM by Medical Diagnostic Technologies, Inc. — Product Code CJE

K952746 is an FDA 510(k) premarket notification submitted by Medical Diagnostic Technologies, Inc. for the device "ALKALINE PHOSPHATASE REAGENT SYSTEM". The FDA issued a decision of Substantially Equivalent on November 27, 1995. The device falls under product code CJE (Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes), a Class II device regulated under 21 CFR 862.1050. Medical Diagnostic Technologies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 27, 1995
Date Received
June 16, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes
Device Class
Class II
Regulation Number
862.1050
Review Panel
CH
Submission Type