Zeus Scientific, Inc.
Zeus Scientific, Inc. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 2022, with 4 FDA device recalls on record.
Clearances by Zeus Scientific, Inc. — page 2
101–135 of 135- K913787 — TOXOPLASMA IGM ELISA TEST SYSTEM
- K900196 — LYME IGM ELISA TEST SYSTEM
- K900743 — CMV-IGM IFA TEST SYSTEM
- K896355 — CMV IGM ELISA TEST SYSTEM
- K897025 — ANTINUCLEAR ANTIBODY (ANA) TEST SYSTEM
- K895292 — LYME IGG ELISA TEST SYSTEM
- K891783 — RUBELLA ELISA TEST SYSTEM
- K891781 — TOXO ELISA TEST SYSTEM
- K891162 — HSV-1 ELISA TEST SYSTEM
- K891782 — HSV-2 ELISA TEST SYSTEM
- K891081 — CMV ELISA TEST SYSTEM
- K885317 — LYME ELISA TEST SYSTEM
- K882440 — EPSTEIN-BARR VIRUS NUCLEAR ANTIGEN ANTIBODY TEST
- K882447 — EPSTEIN-BARR VIRUS EARLY ANTIGEN (EA) ANTIBODY TES
- K871246 — IFA TEST FOR ANTIBODIES TO BORRELIA BURGDORFERI
- K841434 — VARICELLA-ZOSTER(IGG) IFA TEST
- K840221 — EXTRACTABLE NUCLEAR ANTIGEN ASSAY
- K833014 — EBV-VCA-IGM IFA TEST SYSTEM
- K831358 — AUTOANTIBODY SCREEN TEST SYSTEM
- K821060 — FLUORO-CEP
- K811671 — CYTOMEGALOVIRUS ANTIBODY TEST SYSTEM
- K812085 — HERPES VIRUS HOMINIS ANTIBODY TEST SYS.
- K811261 — ANTI-SKIN ANTIBODY TEST SYSTEM
- K811262 — EPSTEIN-BARR VIRUS CAPSID ANTIGEN ANTI
- K791571 — TOXOPLASMA ANTIBODY TEST SYSTEM
- K781516 — TEST SYSTEM TISSUE CELL CULTURE SLIDE
- K781403 — FTA-ABS TEST SYSTEM
- K780178 — TEST SYS. FOR NDNA ANTIBODY DETERM.
- K780161 — IMMUNOPEROXIDASE TEST SYS. FOR ANA SETER
- K761138 — FA TISSUE FIXATIVE & WASH SET
- K760209 — ACID, NATIVE-DEOXYRIBONUCLEIC, IVDP
- K760153 — TEST, (IVDP) ANTINUCLEAR ANTIBODY
- K760154 — TEST, (IVDP) THYROID ANTIBODY
- K760155 — TEST, (IVDP) MITOCHONDRIAL ANTIBODY
- K760156 — TEST, (IVDP) SMOOTHMUSCLE ANTIBODY
Data sourced from openFDA. This site is unofficial and independent of the FDA.