510(k) K896483

QM300 ALPHA2 MACROGLOBULIN ANTIBODY PACK by Kallestad Diag, A Div. of Erbamont, Inc. — Product Code DEB

K896483 is an FDA 510(k) premarket notification submitted by Kallestad Diag, A Div. of Erbamont, Inc. for the device "QM300 ALPHA2 MACROGLOBULIN ANTIBODY PACK". The FDA issued a decision of Substantially Equivalent on December 1, 1989. The device falls under product code DEB (Alpha-2-Macroglobulin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5620. Kallestad Diag, A Div. of Erbamont, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 1, 1989
Date Received
November 13, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Alpha-2-Macroglobulin, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5620
Review Panel
IM
Submission Type