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Arbo Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K940323ARBO DIAGNOSTIC ECG PATIENT CABLES & LEADWIRES ARBO SHIELDED MULTI-LEAD CABLE & LEAD SYSTEMApril 12, 1995
K935437ARBO H85V/H87V/H27V DISPOS MONIT ELECTRODESApril 6, 1995
K942905DISPOSABLE TEMPERATURE PROBE COVERFebruary 27, 1995
K940302ARBO MONITRING SAFETY CABLE & LEAD WIRE SYSTEMS/ARBO UNSHEILDED SAFETY CABLE & LEAD SYSTEMNovember 30, 1994
K940322ARBO VS MONITOR CABLE & LEADWIRE SYSTEM ARBO SHIELDED SAFETY CABLE & LEAD WIRENovember 28, 1994
K935246ARBO H49P, H59P DISPOSABLE MONITORING ELECTRODESNovember 16, 1994
K935429ARBO H90, H91, H135 DISPOSABLE MONITORING ELECTRODESNovember 1, 1994
K935281ARBO H87P, H85P, H27P DISPOSABLE MONITORING ELECTRODESSeptember 6, 1994
K905545ULTRASOUND TRANSMISSION GELMarch 29, 1991
K902788CLEM TMSeptember 12, 1990
K901816PRESSURE TUBING AND ACCESSORIESJuly 12, 1990
K894562ARBO H79P DISPOSABLE MONITORING ELECTRODESSeptember 5, 1989
K894648ARBO TAB DISPOSABLE DIAGNOSTIC RESTING EKG ELECTROSeptember 5, 1989
K892520BREATHING CIRCUIT BACTERIAL FILTERSAugust 2, 1989
K884775ARBO PINK H82PFebruary 6, 1989