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LZF — Pump, Infusion, Analytical Sampling Class II

FDA Device Classification

Classification Details

Product Code
LZF
Device Class
Class II
Regulation Number
880.5725
Submission Type
Review Panel
CH
Medical Specialty
General Hospital
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K192785optiscan biomedical corporationOptiScanner® 5000 Glucose Monitoring SystemFebruary 5, 2020
K162042optiscan biomedicalOptiScanner 5000 Glucose Monitoring SystemOctober 16, 2017
K011238metracor technologiesRODA (REAL TIME OXYGEN DYNAMICS ANALYSIS) MONITORING SYSTEMJanuary 8, 2002
K951739via medicalPUMP/BLOOD CHEMISTRY MONITORFebruary 28, 1996
K922997via medicalVIA 1-01 INFUSION PUMP/BLOOD CHEM. SYST. -- MOD.January 11, 1994
K920438via medicalVIA 1-01 INFUSION PUMP BLOOD CHEMISTRY SYSTEMOctober 22, 1993
K882830pemlabINFUSION PUMPDecember 30, 1988