510(k) K914069

REFLAB(TM) BRAND SYST PK LIQ REAGENT, APOLIPOP A-1 by Medical Analysis Systems, Inc. — Product Code MSJ

K914069 is an FDA 510(k) premarket notification submitted by Medical Analysis Systems, Inc. for the device "REFLAB(TM) BRAND SYST PK LIQ REAGENT, APOLIPOP A-1". The FDA issued a decision of Substantially Equivalent on October 2, 1991. The device falls under product code MSJ (Apolipoproteins), a Class I device regulated under 21 CFR 862.1475. Medical Analysis Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 2, 1991
Date Received
September 11, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Apolipoproteins
Device Class
Class I
Regulation Number
862.1475
Review Panel
CH
Submission Type