Atlas FDA

ONO Retrieval Device

FDA 510(k) clearance K212988 · decided 2022-05-23

Clearance details

K-number
K212988
Device name
ONO Retrieval Device
Applicant
Onocor Vascular, LLC
Decision
Substantially Equivalent
Date received
2021-09-20
Decision date
2022-05-23
Days to decision
245 days
Clearance type
Traditional
Product code
MMX
Device class
2
Regulation number
870.5150
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
West Chester, PA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
LimFlow V-Ceiver (K242776)LimFlow, Inc.2025-02-14
Amplatz Goose Neck Snare Kit (K241259)Medtronic, Inc.2024-06-03
Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit (K232443)Argon Medical Devices, Inc.2023-09-07
Gunther Tulip Vena Cava Filter Retrieval Set (K222254)Cook Incorporated2023-05-16
LimFlow V-Ceiver (K222083)LimFlow, Inc.2022-08-09
Aveir Retrieval Catheter (K213494)ABBOTT MEDICAL2022-04-01
Halo Single-Loop Microsnare Kit (K200963)Argon Medical Devices, Inc.2021-01-05
Halo™ Single-Loop Snare Kit (K200268)Argon Medical Devices, Inc.2020-06-03
Merit ONE Snare System (K193507)Merit Medical Systems, Inc.2020-01-17
Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit (K191758)Argon Medical Devices, Inc.2019-12-17
Günther Tulip® Vena Cava Filter Retrieval Set (K181757)Cook Incorporated2018-11-06
Captus Vascular Retrieval System (K170987)Avantec Vascular Corporation2017-08-28

Recalls involving this device

No recalls on record reference this clearance.