Wampole Laboratories

12 FDA 510(k) medical device clearances.

Top product codes for Wampole Laboratories

Recent clearances by Wampole Laboratories

K965129 — BORRELIA BURGDORFERI IGM ELISA TEST SYSTEM LSR · 1997-03-26
K965131 — BORRELIA BURGDORFERI IGG/IGM ELISA TEST SYSTEM LSR · 1997-03-26
K911444 — RUBELLA VIRUS IMMUNOLOGICAL TEST SYSTEM LFX · 1991-08-30
K882896 — ONE-STEP HCG DHA · 1988-10-31
K883004 — MONO-PLUS(TM) KTN · 1988-08-04
K875101 — VIROGEN CMV ANTIBODY TEST LQO · 1988-03-01
K875161 — MAT (TM) MICROALBUMIN TEST DCF · 1988-02-17
K791309 — UCG-LYPHOTEST JHJ · 1979-07-30
K790986 — RF CONTROLS DMR · 1979-06-28
K781794 — BETA-TEC JHI · 1978-12-29
K760336 — BIOCEPT-G JHI · 1976-11-12
K760681 — INDIRECT FLUORESCENT (IFA-ANA) DHN · 1976-10-21

Data sourced from openFDA. This site is unofficial and independent of the FDA.