510(k) K001569

INFINITY AMYLASE REAGENT (PROCEDURE NO. 580/568) by Sigma Diagnostics, Inc. — Product Code JFJ

K001569 is an FDA 510(k) premarket notification submitted by Sigma Diagnostics, Inc. for the device "INFINITY AMYLASE REAGENT (PROCEDURE NO. 580/568)". The FDA issued a decision of Substantially Equivalent on June 26, 2000. The device falls under product code JFJ (Catalytic Methods, Amylase), a Class II device regulated under 21 CFR 862.1070. Sigma Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 26, 2000
Date Received
May 19, 2000
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