Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Microfilter, Blood Transfusion
510(k) Number K955515
Device Name ALPHA MICRON 20 MICROAGGREGATE FILTER
Applicant
Alpha Therapeutic Corp.
5555 Valley Blvd.
Los Angeles,  CA  90032
Applicant Contact M. SUE PRESTON
Correspondent
Alpha Therapeutic Corp.
5555 Valley Blvd.
Los Angeles,  CA  90032
Correspondent Contact M. SUE PRESTON
Regulation Number880.5440
Classification Product Code
CAK  
Date Received12/04/1995
Decision Date 02/12/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-