Preventive Care, Inc. is one of 5186 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Preventive Care, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Preventive Care, Inc. has 3 FDA 510(k) cleared medical devices. Based in Eagan, US.
Historical record: 3 cleared submissions from 1993 to 2013. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Preventive Care, Inc. Filter by specialty or product code using the sidebar.
Preventive Care, Inc. — FDA 510(k) Products and Clearance History
3 devices
Cleared
Jul 24, 2013
POWDERFREE LATEX EXAMINATION GLOVES COATED WITH ALLOGEL
General Hospital
134d
Cleared
May 13, 2011
POWDERFREE NITRILE EXAMINATION GLOVES COATED WITH ALLOGEL,COLORS...
General Hospital
120d
Cleared
Mar 12, 1993
SAVACARE LATEX EXAMINATION GLOVES
General Hospital
200d