Medical Device Manufacturer · US , Mchenry , IL

Paragon Diagnostics, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1984
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.

7 devices
1–7 of 7
IMMPULSE AMIKACIN ASSAY REAGENTS
K841161 · KLQ Radioimmunoassay, Amikacin · Toxicology
May 1984 44d
IMMPULSE GENTAMICIN ASSAY REAGENTS
K841162 · LCQ Fluorescent Immunoassay Gentamicin · Toxicology
May 1984 44d
IMMPULSE T4 ASSAY REAGENTS
K840852 · CDX Radioimmunoassay, Total Thyroxine · Chemistry
Apr 1984 54d
IMMPULSE THEOPHYLLINE ASSAY REAGENTS
K840758 · LER Fluorescent Immunoassay, Theophylline · Toxicology
Apr 1984 41d
IMMPULSE TOBRAMYCIN ASSAY REAGENTS
K840847 · LCR Fluorescent Immunoassay, Tobramycin · Toxicology
Apr 1984 40d
IMMPULSE TBC ASSAY REAGENTS
K840853 · KHQ Radioassay, Triiodothyronine Uptake · Chemistry
Apr 1984 37d
IMMPULSE SYSTEM
K834070 · JZT Fluorometer · Immunology
Mar 1984 119d
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All7 Toxicology 4 Chemistry 2 Immunology 1