Pascal Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pascal Co., Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Pascal Co., Inc. has 8 FDA 510(k) cleared medical devices. Based in Bellevue, US.
Historical record: 8 cleared submissions from 1991 to 2010. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Pascal Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pascal Co., Inc.
8 devices
Cleared
Oct 22, 2010
BLO2X OXYGEN BLOCKER
Dental
50d
Cleared
Mar 16, 2009
FLUORILAQ SODIUM FLUORIDE CAVITY VARNISH
Dental
11d
Cleared
Jul 07, 2004
ZIRCON-F PROPHYLAXIS PASTE
Dental
83d
Cleared
Jun 09, 2004
RADENT PROPHY PASTE
Dental
89d
Cleared
May 27, 2003
BANICIDE LIQUID CHEMICAL STERILANT/HIGH-LEVEL DISINFECTANT
General Hospital
637d
Cleared
May 02, 2003
FLUORILAQ
Dental
77d
Cleared
Jan 17, 1992
OCCLUDE
Dental
217d
Cleared
Jun 06, 1991
HYDENT
Dental
76d