Premarket Approval (PMA)

Note: this medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original PMA or panel track supplement and may not represent the most recent labeling.

• Device: AB -HAVK
• Generic Name: Hepatitis a test (antibody and igm antibody)
• Regulation Number: 866.3310
• Applicant: DIASORIN; 1951 NORTHWESTERN AVENUE; PO BOX 285; STILLWATER, MN 55082-0285
• PMA Number: P890019
• Date Received: 03/15/1989
• Decision Date: 07/13/1990
• Reclassified Date: 02/09/2006
• Product Code: LOL
• Docket Number: 90m-0245
• Notice Date: 10/01/1990
• Advisory Committee: Microbiology
• Expedited Review Granted?: No
• Combination Product: No
• Supplements: S001 S005 S006 S007 S009 S011 S012