Sancella, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Sancella, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Sancella, Inc. has 5 FDA 510(k) cleared medical devices. Based in Canada, CA.
Historical record: 5 cleared submissions from 1991 to 1991. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Sancella, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sancella, Inc.
5 devices
Cleared
Oct 04, 1991
MEDI GUARD DENTAL BIB
General Hospital
156d
Cleared
May 28, 1991
MEDI GUARD PILLOWCASE
General Hospital
27d
Cleared
May 28, 1991
MEDI GUARD UNDERPAD
General Hospital
27d
Cleared
May 28, 1991
MEDI GUARD SHEETS/UNDERLAYS
General Hospital
27d
Cleared
May 21, 1991
MEDI GUARD DRAPES
General Hospital
20d