Wampole Laboratories
Wampole Laboratories holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1997.
Top product codes for Wampole Laboratories
Recent clearances by Wampole Laboratories
- K965129 — BORRELIA BURGDORFERI IGM ELISA TEST SYSTEM
- K965131 — BORRELIA BURGDORFERI IGG/IGM ELISA TEST SYSTEM
- K911444 — RUBELLA VIRUS IMMUNOLOGICAL TEST SYSTEM
- K882896 — ONE-STEP HCG
- K883004 — MONO-PLUS(TM)
- K875101 — VIROGEN CMV ANTIBODY TEST
- K875161 — MAT (TM) MICROALBUMIN TEST
- K791309 — UCG-LYPHOTEST
- K790986 — RF CONTROLS
- K781794 — BETA-TEC
- K760336 — BIOCEPT-G
- K760681 — INDIRECT FLUORESCENT (IFA-ANA)
Data sourced from openFDA. This site is unofficial and independent of the FDA.