Simplicity Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Simplicity Diagnostics, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Simplicity Diagnostics, Inc. has 5 FDA 510(k) cleared medical devices. Based in Hatboro, US.
Historical record: 5 cleared submissions from 1992 to 1997. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Simplicity Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Simplicity Diagnostics, Inc.
5 devices
Cleared
Mar 10, 1997
TECH SIMPLE SYPHILIS POSITIVE SERUM CONTROL MONITOR ONTRAK SYPHILIS POSITIVE...
Microbiology
59d
Cleared
Oct 05, 1992
TECH DIMPLE C-REACTIVE PROTEIN SERUM CONTROL
Immunology
122d
Cleared
Oct 05, 1992
TECH SIMPLE RHEUMATOID FACTOR SERUM CONTROL
Immunology
122d
Cleared
Oct 05, 1992
TECH SIMPLE INFECTIOUS MONONUCLEOSIS SERUM CONTROL
Immunology
122d
Cleared
Sep 18, 1992
TECH SIMPLE ANTISTREPTOLYSIN O ASO SERUM CONTROL
Microbiology
105d