Atlas FDA

POWER-TRIALYSIS SHORT-TERM DIALYSIS CATHETER

FDA 510(k) clearance K133456 · decided 2014-09-24

Clearance details

K-number
K133456
Device name
POWER-TRIALYSIS SHORT-TERM DIALYSIS CATHETER
Applicant
C.R. Bard, Inc.
Decision
Unknown
Date received
2013-11-12
Decision date
2014-09-24
Days to decision
316 days
Clearance type
Traditional
Product code
NIE
Device class
2
Regulation number
876.5540
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Salt Lake Ciy,, UT, US
Third-party review
No
Expedited review
No

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Multi-Lumen Acute Hemodialysis Catheter for High Volume Infusions (K143102)Arrow International, Inc. (Subsidiary of Teleflex, Inc.)2015-07-24
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Recalls involving this device

RecordFirmDate
5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Co recall (Z-2660-2026)Bard Access Systems, Inc.2026-07-02

PMA approvals by this applicant

RecordFirmDate
Covera™ Vascular Covered Stent (P170042/S014)C.R. Bard, Inc.2025-12-16
Covera™ Vascular Covered Stents (P170042/S013)C.R. Bard, Inc.2025-06-26
Avitene Microfibrillar Collagen Hemostat (P800002/S033)C.R. Bard, Inc.2025-03-13
AVITENE MICROFIBRILLAR COLLAGEN HEMOSTAT NON-WOVEN WEB (P800002/S032)C.R. Bard, Inc.2025-02-18
Avitene™ Bulk Flour Cleanroom Expansion (P800002/S031)C.R. Bard, Inc.2024-01-18
Avitene™ Microfibrillar Collagen Hemostat (P800002/S030)C.R. Bard, Inc.2023-10-04
Covera™ Vascular Covered Stent (P170042/S012)C.R. Bard, Inc.2023-02-02
Avitene Microfibrillar Collagen Hemostat (MCH) Non-Woven Web and Avitene Microfibrillar Collagen Hemostat (MCH) EndoAvit (P800002/S027)C.R. Bard, Inc.2022-04-01