Jelco Laboratories

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
26
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K791918JELCO WINGED INTRAVASCULAR CATHETEROctober 2, 1979
K791372JELCO & KVO CATHETER PLACEMENT UNITSeptember 12, 1979
K790967CATHETER METAL HUB/RADIOPAQUEJune 27, 1979
K790968CATHETER METAL HUB/NONRADIOPAQUEJune 11, 1979
K790471JELCO* DISC FILTER-0.2 MICRONApril 30, 1979
K790186PROTECTIVSTABILIZERFebruary 26, 1979
K790107CATHETER TUBING MODIFICATIONFebruary 1, 1979
K790079NEEDLE, BLOOD COLLECTINGFebruary 1, 1979
K781857TRAY, ARTERIAL BLOOD GAS SAMPLINGDecember 11, 1978
K780896NEEDLES, DESIGN CHANGE, IV CATHETERSAugust 23, 1978
K780519FILTER TUBEMay 9, 1978
K771874J-VAC VACUUM TUBEDecember 2, 1977
K771536AIR VENT FILTER NEEDLE, 0.45October 25, 1977
K771381IV CATHETER HUBOctober 13, 1977
K771826INTRAVENOUS FILTER W/AUTO AIR VENTOctober 13, 1977
K771827INTRAVENOUS FILTER W/FLASH BULBOctober 13, 1977
K771551I.V. PREP & CARE KITOctober 4, 1977
K770589FILTER, INTRAVENOUS W/AUTO AIR VENTMay 23, 1977
K770119I.V. LOK TMMarch 14, 1977
K760319KIT, CATHETERAugust 11, 1976