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Medimop Medical Projects Ltd.

FDA Regulatory Profile

Summary

Total Recalls
1
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0972-2018Class IIVial2BagDC, Product Number 6070112. The 20mm Vial2Bag DC device, is intended for use in healthcarOctober 6, 2017

Recent 510(k) Clearances

K-NumberDeviceDate
K160503Vented Vial Adapter Transfer Device - 13mmMay 4, 2016
K140730VIAL2BAG DIRECT CONNECTJune 12, 2014
K130179MP VIAL ADAPTER 13MMAugust 8, 2013
K132040VIAL CONNECTOR 13MM CLOSED COLLARJuly 31, 2013
K122023MIXJECT WITH SPRAY HEADOctober 4, 2012
K072511SWABABLE VIAL ADAPTER 13MM, SWABABLE VIAL ADAPTER 20MMDecember 13, 2007
K072759VIAL2BAGDecember 13, 2007
K062482VENTED VIAL ADAPTER TRANSFER DEVICENovember 3, 2006
K031861MIX2VIAL TRANSFER DEVICEJuly 29, 2003
K001831NEEDLELESS TRANSFER DEVICEJuly 11, 2000
K001293MODIFICATION TO MIXJECT DISPENSING PIN/WITH DETACHABLE VIAL HOLDER/WITH DETACHABLE VIAL HOLDER AND PMay 5, 2000
K963583MIXJECT DISPENSING PIN/WITH DETACHABLE VIAL HOLDER/WITH DETACHABLE VIAL HOLDER AND PREATTACHED NEEDLOctober 7, 1996