FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

MIXJECT WITH SPRAY HEAD

K Number: K122023 · Decision Oct 4, 2012
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
12
Review Days
85

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Basic Information

Device Name
MIXJECT WITH SPRAY HEAD
K Number
K122023
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medimop Medical Projects, Ltd.
Date Received
July 11, 2012
Decision Date
October 4, 2012
Product Code
FMF
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FMF Syringe, Piston

Similar 510(k) Clearances

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Other Clearances by Medimop Medical Projects, Ltd.

K Number Device Name
K160503 Vented Vial Adapter Transfer Device - 13mm
K140730 VIAL2BAG DIRECT CONNECT
K130179 MP VIAL ADAPTER 13MM
K132040 VIAL CONNECTOR 13MM CLOSED COLLAR
K072511 SWABABLE VIAL ADAPTER 13MM, SWABABLE VIAL ADAPTER 20MM
K072759 VIAL2BAG
K062482 VENTED VIAL ADAPTER TRANSFER DEVICE
K031861 MIX2VIAL TRANSFER DEVICE
K001831 NEEDLELESS TRANSFER DEVICE
K001293 MODIFICATION TO MIXJECT DISPENSING PIN/WITH DETACHABLE VIAL HOLDER/WITH DETACHABLE VIAL HOLDER AND PRE-ATTACHED NEEDLE
Search all 12 clearances from Medimop Medical Projects, Ltd. →