Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

ONB — Predicate Candidate Screening

41 FDA 510(k) clearances under this product code; the 50 most recent screened below.

175 daysmedian FDA review time
307 days90th percentile
41clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K251722ProSeal™ Transfer Injector (421120, 421130, 421140)Epic Medical Pte. , Ltd.2025-12-051840
K253033Chemfort® 28-day 20 mm Vial Adaptor and 13 mm ConvertorSimplivia Healthcare , Ltd.2025-10-21290
K250059BD PhaSeal™ Optima Connecting Set (C83-O); BD PhaSeal™ OptimBecton, Dickinson and Company2025-09-122450
K251411Chemfort Female Luer Lock AdaptorSimplivia Healthcare , Ltd.2025-08-05900
K251340ProSeal™ Bag Spike with Additive Port (423370ST, 423370)Epic Medical Pte. , Ltd.2025-05-29290
K243976ZeroClear™ Bag Access (423100)Epic Medical Pte. , Ltd.2025-01-22300
K240517ProSeal™ Vented Universal Vial AdaptorEpic Medical Pte. , Ltd.2024-12-263070
K241988ProSeal™ Closed System Bag AccessEpic Medical Pte. , Ltd.2024-10-231070
K241735ProSeal™ In Line Pump Set (423850)Epic Medical Pte. , Ltd.2024-10-101150
K241823ToxiSeal™ Vial AdaptorEpic Medical Pte. , Ltd.2024-08-30670
K241476ToxiSeal™ Vial Adaptor with External Flip BalloonEpic Medical Pte. , Ltd.2024-06-21280
K240433ProSeal™ Injection Site Extended Male Luer Lock (422140)Epic Medical Pte. , Ltd.2024-05-21970
K240171ProSeal™ Injector Plus (Model no. 421050)Epic Medical Pte. , Ltd.2024-03-28660
K222929ToxiSeal Vial Adapter with External BalloonEpic Medical Pte. , Ltd.2024-01-114720
K231286Chemfort® Catheter AdaptorSimplivia Healthcare , Ltd.2023-08-02900
K223076BD Texium™ Closed Male LuerCare Fusion2023-03-241750
K221513Equashield Closed System Transfer DeviceEquashield Medical , Ltd.2023-02-172680
K201460Closed System Transfer DeviceShinva Ande Healthcare Apparatus Co., Ltd.2022-11-239040
K210707OnGuard2 Chemfort Closed Administration (CADM)Simplivia Healthcare , Ltd.2021-09-231970
K201422Arisure Closed System Drug Transfer Device (CSTD)Yukon Medical, LLC2021-03-022770
K201142TEVADAPTOR Bag Adaptor LL, TEVADAPTOR Bag Adaptor LL with ULSimplivia Healthcare , Ltd.2021-02-253020
K201099BD PhaSeal Optima Closed System Drug Transfer DeviceBecton, Dickinson and Company2020-08-121101
K192075ProSeal™ Closed System drug Transfer Device (CSTD)Epic Medical Pte. , Ltd.2020-08-073710
K192866Chemfort CSTDSimplivia Healthcare , Ltd.2020-05-072130
K190157Diana ChemoClave Transfer SetIcu Medical2019-10-232660
K181221BD PhaSeal Optima Closed System Transfer DeviceBecton, Dickinson and Company2018-11-302071
K180489TEVADAPTOR Closed Drug Reconstitution and Transfer SystemTeva Medical Ltd., Migada Plant2018-09-212100
K173477ChemoCLAVE Cytotoxic Medication Preparation and Delivery SysIcu Medical, Inc.2018-08-312910
K180574Halo Closed Vial Adaptor (Multiple Models based on 13, 20 orJ & J Solutions, Inc. D/B/A/ Corvida Medical2018-08-171650
K170110Diana Medication Transfer SetIcu Medical, Inc.2018-08-105750
K172499NEOSHIELDJMS North America Corporation2018-06-012870
K170706Equashield Closed System drug Transfer Device (CSTD)Equashield Medical , Ltd.2017-07-031170
K170680TEVADAPTOR Closed Drug Reconstitution and Transfer SystemTeva Medical Ltd., Migada Plant2017-05-16710
K150219Equashield Closed System drug Transfer Device (CSTD)Equashield Medical , Ltd.2015-11-052790
K150486HaloJ & J Solutions, Inc. D/B/A/ Corvida Medical2015-07-241500
K141448TEVADAPTOR CLOSED DRUG RECONSTITUTION AND TRANSFER SYSTEMTeva Medical Ltd., Migada Plant2015-01-232350
K140591BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE - INJECTORBecton, Dickinson & CO2014-05-14681
K132899EQUASHIELD CLOSED SYSTEM DRUG TRANSFER DEVICE (CSTD)Equashield Medical , Ltd.2014-05-132390
K131549CHEMOLOCK, CHEMOLOCK PORTIcu Medical, Inc.2013-07-265842
K130197BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE - P55Becton, Dickinson and Company2013-02-27301
K123213BD PHASEAL CLOSED SYSTEM TRANSFER DEVICEBecton, Dickinson & CO2013-01-09861

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda