Atlas FDA

Bard Mission Disposable Core Biopsy Instrument

FDA 510(k) clearance K171953 · decided 2017-09-14

Clearance details

K-number
K171953
Device name
Bard Mission Disposable Core Biopsy Instrument
Applicant
Bard Peripheral Vascular, Inc.
Decision
Substantially Equivalent
Date received
2017-06-29
Decision date
2017-09-14
Days to decision
77 days
Clearance type
Traditional
Product code
KNW
Device class
2
Regulation number
876.1075
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Tempe, AZ, US
Third-party review
Yes
Expedited review
No

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Recalls involving this device

RecordFirmDate
Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x recall (Z-0643-2024)Bard Peripheral Vascular Inc2024-01-05
Bard Mission Disposable Core Biopsy Instrument Kit: REF: 2010MSK, 20G x 10CM; REF: 2016MSK recall (Z-1564-2023)Bard Peripheral Vascular Inc2023-05-05
Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM, REF: 1610MSK; 18G x 16CM, recall (Z-1260-2023)Bard Peripheral Vascular Inc2023-03-16

PMA approvals by this applicant

RecordFirmDate
LifeStent® Vascular Stent Systems (P070014/S066)Bard Peripheral Vascular, Inc.2025-12-16
LifeStream™ Balloon Expandable Vascular Covered Stent (P160024/S014)Bard Peripheral Vascular, Inc.2025-09-29
FLUENCY PLUS ENDOVASCULAR STENT GRAFT (P130029/S013)Bard Peripheral Vascular, Inc.2025-08-13
Venovo Venous Stent System (P180037/S014)Bard Peripheral Vascular, Inc.2024-12-06
LifeStream Balloon Expandable Vascular Covered Stent (P160024/S013)Bard Peripheral Vascular, Inc.2024-12-06
LifeStent Vascular Stent System (P070014/S065)Bard Peripheral Vascular, Inc.2023-07-27
Fluency™ Endovascular Stent Graft (P130029/S012)Bard Peripheral Vascular, Inc.2023-02-17
LifeStent™ 5F Vascular Stent Systems (P070014/S064)Bard Peripheral Vascular, Inc.2023-02-02