Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ERIC Retrieval Device

K-Number: K211120 · 2022-03-31

ApplicantMicroVention, Inc.
Decision Date2022-03-31
Product CodeNRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ERIC Retrieval Device is a medical device manufactured by MicroVention, Inc.. It received FDA 510(k) clearance on 2022-03-31 under approval number K211120. The device is classified under product code NRY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ERIC Retrieval Device?

ERIC Retrieval Device is a medical device that received FDA 510(k) clearance on 2022-03-31. It is manufactured by MicroVention, Inc.. The 510(k) number is K211120.

When was ERIC Retrieval Device approved by the FDA?

ERIC Retrieval Device received FDA 510(k) clearance on 2022-03-31, under approval number K211120.

What company makes ERIC Retrieval Device?

ERIC Retrieval Device is manufactured by MicroVention, Inc..

What is the FDA product code for ERIC Retrieval Device?

The FDA product code for ERIC Retrieval Device is NRY.

Related Clinical Trials

NCT07356284 Emergent Large Vessel Occlusion Endovascular Rescue Therapy With Underlying Intracranial Stenosis RECRUITING NCT07042061 Trial of Mobile External Defibrillator for Out-of-hospital Cardiac Arrest in Singapore. NOT_YET_RECRUITING NCT04213781 Interest of Audiovisual Distraction in the Management of Anxiety and Pain During Oocyte Retrieval COMPLETED NCT07512973 Single-channel Fibroid Morcellation System Used in Clinical Research on Laparoscopic Myomectomy NOT_YET_RECRUITING

Related PubMed Literature

PMID: 41915420 Analysis Model for Infant Incubator Adverse Events Using Retrieval-Augmented Generation Combined With Dual-Adapter Fine-Tuning: Development and Evaluation Study. JMIR medical informatics (2026)

Other Devices by MicroVention, Inc.

K163154Traxcess 7 Mini XSoft Guidewire K161803Traxcess .007 Mini Guidewire K161367HydroCoil Embolic System (HES) K161452MicroPlex Coil System (MCS) - HyperSoft 3D K153594MicroPlex Coil System (MCS), Hydrocoil Embolic System (HES) K162999V-Grip Detachment Controller for use with Hydrocoil Embolic System and MicroPlex Coil System, AZUR Detachment Controller for use with AZUR Peripheral Coil System

View all 28 devices →

Related Devices (Code: NRY)

K161879Solitaire Platinum Revascularization DeviceMicro Therapeutics, Inc. d/b/a ev3 Neurovascular K161640Penumbra System ACE 68 Reperfusion CatheterPenumbra, Inc. K161064Penumbra System ACE 68 Reperfusion CatheterPenumbra, Inc. K160449Penumbra System, Penumbra Pump MAXPenumbra, Inc. K152541Penumbra System ACE 64 and ACE 68 Reperfusion CathetersPenumbra, Inc. K172448Riptide Aspiration SystemMicro Therapeutics, Inc. d/b/a ev3 Neurovascular

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑