510(k) K942640

DUPONT DIMENSION AMYLASE METHOD by Dupont Medical Products — Product Code JFJ

K942640 is an FDA 510(k) premarket notification submitted by Dupont Medical Products for the device "DUPONT DIMENSION AMYLASE METHOD". The FDA issued a decision of Substantially Equivalent on September 9, 1994. The device falls under product code JFJ (Catalytic Methods, Amylase), a Class II device regulated under 21 CFR 862.1070. Dupont Medical Products has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 9, 1994
Date Received
June 3, 1994
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