510(k) K880867

AMYLASE 405 CATALOG NUMBER 301-34 by Diagnostic Chemicals, Ltd. (Usa) — Product Code JFJ

K880867 is an FDA 510(k) premarket notification submitted by Diagnostic Chemicals, Ltd. (Usa) for the device "AMYLASE 405 CATALOG NUMBER 301-34". The FDA issued a decision of Substantially Equivalent on April 19, 1988. The device falls under product code JFJ (Catalytic Methods, Amylase), a Class II device regulated under 21 CFR 862.1070. Diagnostic Chemicals, Ltd. (Usa) has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 19, 1988
Date Received
March 1, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catalytic Methods, Amylase
Device Class
Class II
Regulation Number
862.1070
Review Panel
CH
Submission Type