FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ALPHA MICRON-40 FILTER

K Number: K810761 · Decision Jun 30, 1981
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
35
Applicant Total
8
Review Days
102

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ALPHA MICRON-40 FILTER
K Number
K810761
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Alpha Therapeutic Corp.
Date Received
March 20, 1981
Decision Date
June 30, 1981
Product Code
CAK
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CAK Microfilter, Blood Transfusion

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CAK), ordered by most recent decision date.

View all

Other Clearances by Alpha Therapeutic Corp.

K Number Device Name
K970225 ALPHA MICRON 20/40 MICROAGGREGATE FILTER
K955515 ALPHA MICRON 20 MICROAGGREGATE FILTER
K854920 THERAPY CASSETTS
K854441 STUART GILMAN'S WEIGHT LOSS PLAN
K833294 ALPHA Y-RECIPIENT SET
K820447 ALPHA PLASMA TRANSFER SET
K810897 ALPHA PLASTIC PLASMA BOTTLE