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

TEVADAPTOR Closed Drug Reconstitution and Transfer System

K Number: K170680 · Decision May 16, 2017
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
40
Applicant Total
4
Review Days
71

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Basic Information

Device Name
TEVADAPTOR Closed Drug Reconstitution and Transfer System
K Number
K170680
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Teva Medical Ltd., Migada Plant
Date Received
March 6, 2017
Decision Date
May 16, 2017
Product Code
ONB
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
ONB Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System

Similar 510(k) Clearances

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

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Other Clearances by Teva Medical Ltd., Migada Plant

K Number Device Name
K180489 TEVADAPTOR Closed Drug Reconstitution and Transfer System
K141448 TEVADAPTOR CLOSED DRUG RECONSTITUTION AND TRANSFER SYSTEM
K141306 TEVADAPTOR; CONNECTING SET W/ ULTRASITE INJECTION SITE, SPIKE PORT ADAPTOR SET W/ ULTRASITE INJECTION SITE