510(k) K931986

AMP ALKALINE PHOSPHATASE REAGENT KIT by Synermed, Inc. — Product Code CJE

K931986 is an FDA 510(k) premarket notification submitted by Synermed, Inc. for the device "AMP ALKALINE PHOSPHATASE REAGENT KIT". The FDA issued a decision of Substantially Equivalent on September 8, 1993. The device falls under product code CJE (Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes), a Class II device regulated under 21 CFR 862.1050. Synermed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 8, 1993
Date Received
April 22, 1993
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