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

Vial Adapter 15mm

K Number: K171796 · Decision Oct 12, 2017
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
205
Applicant Total
2
Review Days
118

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
Vial Adapter 15mm
K Number
K171796
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medimop Medical Project , Ltd.
Date Received
June 16, 2017
Decision Date
October 12, 2017
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 Project , Ltd.

K Number Device Name
K170095 Vial2Bag Direct Connect