510(k) K861638

KINETIC ALKALINE PHOSPHATASE REAGENT KIT by Bio-Analytics Laboratories, Inc. — Product Code CJE

K861638 is an FDA 510(k) premarket notification submitted by Bio-Analytics Laboratories, Inc. for the device "KINETIC ALKALINE PHOSPHATASE REAGENT KIT". The FDA issued a decision of Substantially Equivalent on May 29, 1986. The device falls under product code CJE (Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes), a Class II device regulated under 21 CFR 862.1050. Bio-Analytics Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 29, 1986
Date Received
April 30, 1986
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