Paragon Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Paragon Diagnostics, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Paragon Diagnostics, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1984 to 1984. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Paragon Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Paragon Diagnostics, Inc.
7 devices
Cleared
May 02, 1984
IMMPULSE AMIKACIN ASSAY REAGENTS
Toxicology
44d
Cleared
May 02, 1984
IMMPULSE GENTAMICIN ASSAY REAGENTS
Toxicology
44d
Cleared
Apr 18, 1984
IMMPULSE T4 ASSAY REAGENTS
Chemistry
54d
Cleared
Apr 04, 1984
IMMPULSE THEOPHYLLINE ASSAY REAGENTS
Toxicology
41d
Cleared
Apr 04, 1984
IMMPULSE TOBRAMYCIN ASSAY REAGENTS
Toxicology
40d
Cleared
Apr 01, 1984
IMMPULSE TBC ASSAY REAGENTS
Chemistry
37d
Cleared
Mar 23, 1984
IMMPULSE SYSTEM
Immunology
119d