510(k) K860530

AMYLASE REAGENT SET (MODIFIED CARAWAY) by Sterling Diagnostics, Inc. — Product Code CJA

K860530 is an FDA 510(k) premarket notification submitted by Sterling Diagnostics, Inc. for the device "AMYLASE REAGENT SET (MODIFIED CARAWAY)". The FDA issued a decision of Substantially Equivalent on February 28, 1986. The device falls under product code CJA (Amyloclastic, Amylase), a Class II device regulated under 21 CFR 862.1070. Sterling Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 28, 1986
Date Received
February 12, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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