510(k) K810761

ALPHA MICRON-40 FILTER by Alpha Therapeutic Corp. — Product Code CAK

K810761 is an FDA 510(k) premarket notification submitted by Alpha Therapeutic Corp. for the device "ALPHA MICRON-40 FILTER". The FDA issued a decision of Substantially Equivalent on June 30, 1981. The device falls under product code CAK (Microfilter, Blood Transfusion), a Class II device regulated under 21 CFR 880.5440. Alpha Therapeutic Corp. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 30, 1981
Date Received
March 20, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Microfilter, Blood Transfusion
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type