510(k) K873386

TITAN GEL LDH REP SYSTEM by Helena Laboratories — Product Code CFE

K873386 is an FDA 510(k) premarket notification submitted by Helena Laboratories for the device "TITAN GEL LDH REP SYSTEM". The FDA issued a decision of Substantially Equivalent on October 20, 1987. The device falls under product code CFE (Electrophoretic, Lactate Dehydrogenase Isoenzymes), a Class II device regulated under 21 CFR 862.1445. Helena Laboratories has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 20, 1987
Date Received
August 24, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrophoretic, Lactate Dehydrogenase Isoenzymes
Device Class
Class II
Regulation Number
862.1445
Review Panel
CH
Submission Type