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

MIX2VIAL TRANSFER DEVICE

K Number: K031861 · Decision Jul 29, 2003
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
205
Applicant Total
12
Review Days
43

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MIX2VIAL TRANSFER DEVICE
K Number
K031861
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medimop Medical Projects, Ltd.
Date Received
June 16, 2003
Decision Date
July 29, 2003
Product Code
LHI
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
LHI Set, I.V. Fluid Transfer

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LHI), ordered by most recent decision date.

View all

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
K122023 MIXJECT WITH SPRAY HEAD
K072511 SWABABLE VIAL ADAPTER 13MM, SWABABLE VIAL ADAPTER 20MM
K072759 VIAL2BAG
K062482 VENTED VIAL ADAPTER 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. →