510(k) K791340

HUMAN ALPHA2 MACROGLOBULIN by Beckman Instruments, Inc. — Product Code DEB

K791340 is an FDA 510(k) premarket notification submitted by Beckman Instruments, Inc. for the device "HUMAN ALPHA2 MACROGLOBULIN". The FDA issued a decision of Substantially Equivalent on August 16, 1979. The device falls under product code DEB (Alpha-2-Macroglobulin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5620. Beckman Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 16, 1979
Date Received
July 16, 1979
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