FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇬 Singapore

ToxiSeal™ Vial Adaptor

K Number: K241823 · Decision Aug 30, 2024
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
40
Applicant Total
22
Review Days
67

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Basic Information

Device Name
ToxiSeal™ Vial Adaptor
K Number
K241823
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Epic Medical Pte. , Ltd.
Date Received
June 24, 2024
Decision Date
August 30, 2024
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 Epic Medical Pte. , Ltd.

K Number Device Name
K252987 ADRx™ Admixture Device
K250234 SMARTeZ™ Elastomeric Infusion Pump (RS series)
K251722 ProSeal™ Transfer Injector (421120, 421130, 421140)
K251814 EZ™ IV Administration Set
K252094 eZSURE™ Empty Fluid Container
K251340 ProSeal™ Bag Spike with Additive Port (423370ST, 423370)
K243976 ZeroClear™ Bag Access (423100)
K240517 ProSeal™ Vented Universal Vial Adaptor
K241988 ProSeal™ Closed System Bag Access
K241735 ProSeal™ In Line Pump Set (423850)
Search all 22 clearances from Epic Medical Pte. , Ltd. →