Atlas FDA

BARD(R) WILLIAM HARVEY(R) ARTERIAL STRAIGH CANNULA

FDA 510(k) clearance K930620 · decided 1993-05-07

Clearance details

K-number
K930620
Device name
BARD(R) WILLIAM HARVEY(R) ARTERIAL STRAIGH CANNULA
Applicant
C.R. Bard, Inc.
Decision
Substantially Equivalent
Date received
1993-02-08
Decision date
1993-05-07
Days to decision
88 days
Clearance type
Traditional
Product code
DWF
Device class
2
Regulation number
870.4210
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Tewksbury, MA, US
Third-party review
No
Expedited review
No

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

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Recalls involving this device

RecordFirmDate
Terumo L Series 1863 type arterial perfusion cannulae, straight open tip, 1/4'' connector, recall (Z-0543-2007)Terumo Cardiovascular Systems Corp2007-02-27
Terumo L Series 1863 type arterial perfusion cannulae, straight open tip, 1/4'' connector, recall (Z-0544-2007)Terumo Cardiovascular Systems Corp2007-02-27

PMA approvals by this applicant

RecordFirmDate
Avitene Microfibrillar Collagen Hemostat (MCH) Non-Woven Web (P800002/S035)C.R. Bard, Inc.2026-07-15
Covera™ Vascular Covered Stent (P170042/S015)C.R. Bard, Inc.2026-06-10
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