510(k) K914262

ABBOTT QUICKSTART LDH,#5A31 by Em Diagnostic Systems, Inc. — Product Code CFJ

K914262 is an FDA 510(k) premarket notification submitted by Em Diagnostic Systems, Inc. for the device "ABBOTT QUICKSTART LDH,#5A31". The FDA issued a decision of Substantially Equivalent on October 11, 1991. The device falls under product code CFJ (Nad Reduction/Nadh Oxidation, Lactate Dehydrogenase), a Class II device regulated under 21 CFR 862.1440. Em Diagnostic Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 11, 1991
Date Received
September 23, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Nad Reduction/Nadh Oxidation, Lactate Dehydrogenase
Device Class
Class II
Regulation Number
862.1440
Review Panel
CH
Submission Type