ToxiSeal Vial Adaptor
FDA 510(k) K241823 · Epic Medical Pte. , Ltd.
510(k) numberK241823
Submission
- Device name
- ToxiSeal Vial Adaptor
- Applicant
- Epic Medical Pte. , Ltd.
Singapore, SG - Received
- June 24, 2024
- Decision date
- August 30, 2024
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- ONB – Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5440
- Specialty
- General Hospital
Reconstitute and transfer antineoplastic and other hazardous drugs in healthcare setting indicated to reduce exposure of healthcare personnel to chemotherapy agents in healthcare setting.
Other 510(k)s with product code ONB
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K251722 | ProSeal Transfer Injector (421120, 421130, 421140)ONB · Special | Epic Medical Pte. , Ltd. | 12/05/2025SE |
| K253033 | Chemfort® 28-day 20 mm Vial Adaptor and 13 mm ConvertorONB · Special | Simplivia Healthcare , Ltd. | 10/21/2025SE |
| K250059 | BD PhaSeal Optima Connecting Set (C83-O); BD PhaSeal Optima Spike Set (C180-O)ONB · Traditional | Becton, Dickinson and Company | 09/12/2025SE |
| K251411 | Chemfort Female Luer Lock AdaptorONB · Traditional | Simplivia Healthcare , Ltd. | 08/05/2025SE |
| K251340 | ProSeal Bag Spike with Additive Port (423370ST, 423370)ONB · Special | Epic Medical Pte. , Ltd. | 05/29/2025SE |
| K243976 | ZeroClear Bag Access (423100)ONB · Special | Epic Medical Pte. , Ltd. | 01/22/2025SE |
| K240517 | ProSeal Vented Universal Vial AdaptorONB · Traditional | Epic Medical Pte. , Ltd. | 12/26/2024SE |
| K241988 | ProSeal Closed System Bag AccessONB · Traditional | Epic Medical Pte. , Ltd. | 10/23/2024SE |
| K241735 | ProSeal In Line Pump Set (423850)ONB · Special | Epic Medical Pte. , Ltd. | 10/10/2024SE |
| K241476 | ToxiSeal Vial Adaptor with External Flip BalloonONB · Special | Epic Medical Pte. , Ltd. | 06/21/2024SE |
More from Epic Medical Pte. , Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K252987 | ADRx Admixture DeviceLHI · Traditional | 06/12/2026SE |
| K250234 | SMARTeZ Elastomeric Infusion Pump (RS series)MEB · Traditional | 04/24/2026SE |
| K251722 | ProSeal Transfer Injector (421120, 421130, 421140)ONB · Special | 12/05/2025SE |
| K251814 | EZ IV Administration SetFPA · Traditional | 08/29/2025SE |
| K252094 | eZSURE Empty Fluid ContainerKPE · Special | 08/01/2025SE |
| K251340 | ProSeal Bag Spike with Additive Port (423370ST, 423370)ONB · Special | 05/29/2025SE |
| K243976 | ZeroClear Bag Access (423100)ONB · Special | 01/22/2025SE |
| K240517 | ProSeal Vented Universal Vial AdaptorONB · Traditional | 12/26/2024SE |
| K241988 | ProSeal Closed System Bag AccessONB · Traditional | 10/23/2024SE |
| K241735 | ProSeal In Line Pump Set (423850)ONB · Special | 10/10/2024SE |
Questions and answers
When was ToxiSeal Vial Adaptor cleared by the FDA?
ToxiSeal Vial Adaptor (K241823) received a 510(k) decision of Substantially Equivalent on August 30, 2024, 67 days after the submission was received.
What is the product code of K241823?
The FDA product code is ONB – Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System, a Class II (moderate risk) device regulated under 21 CFR 880.5440.