Atlas FDA

Ellipsys Vascular Access System (Ellipsys System), Power Controller, Ellipsys Vascular Access System (Ellipsys System), Catheter, Ellipsys Vascular Access System (Ellipsys System), Needle

FDA 510(k) clearance K191114 · decided 2019-08-09

Clearance details

K-number
K191114
Device name
Ellipsys Vascular Access System (Ellipsys System), Power Controller, Ellipsys Vascular Access System (Ellipsys System), Catheter, Ellipsys Vascular Access System (Ellipsys System), Needle
Applicant
Avenu Medical
Decision
Substantially Equivalent
Date received
2019-04-26
Decision date
2019-08-09
Days to decision
105 days
Clearance type
Traditional
Product code
PQK
Device class
2
Regulation number
870.1252
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
San Juan Capistrano, CA, 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
WavelinQ Plus EndoAVF System (K192239)C.R. Bard, Inc.2019-10-17
WavelinQ 4F EndoAVF System (K182796)C.R. Bard, Inc.2019-02-06
Ellipsys Vascular Access System (Ellipsys System), Power Controller, Ellipsys Vascular Access System (Ellipsys System), Catheter, Ellipsys Vascular Access System (Ellipsys System), Crossing Needle (K183615)Avenu Medical, Inc.2019-01-25
Ellipsys Vascular Access System (Ellipsys System), (Power Controller Model No. AMI-1001 & Catheter & Needle Model No. AMI-6005) (K181725)Avenu Medical, Inc.2018-10-05
Ellipsys Vascular Access System (DEN170004)Avenu Medical, Inc.2018-06-22
everlinQ endoAVF System (DEN160006)Tva Medical, Inc.2018-06-22

Recalls involving this device

No recalls on record reference this clearance.