Atlas FDA

ADVANSET

FDA 510(k) clearance K771261 · decided 1977-08-16

Clearance details

K-number
K771261
Device name
ADVANSET
Applicant
C.R. Bard, Inc.
Decision
Substantially Equivalent
Date received
1977-07-11
Decision date
1977-08-16
Days to decision
36 days
Clearance type
Traditional
Product code
DRC
Device class
2
Regulation number
870.1390
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch C.R. Bard

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

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

RecordFirmDate
Accusafe Transseptal Guidewire (GTR31180, GTR31230) (K240246)Synaptic Medical Corporation2024-07-26
SafeSharp Transseptal Needle (CLICK071, CLICK171, CLICK098, CLICK198) (K241042)Pressure Products Medical Device Manufacturing, LLC2024-05-17
SafeSept® Transseptal Guidewire (SS-140) (K221707)Pressure Products Medical Device Manufacturing, LLC2022-09-14
PathBuilder Transseptal Needle (K212625)Shanghai Microport EP Medtech Co., Ltd.2022-03-23
SafeSept Blunt Needle (K210328)Pressure Products Medical Device Manufacturing, LLC2021-03-05
TSN Transseptal Needle (K172950)Pressure Products Medical Device Manufacturing, LLC2018-02-21
Needle Free Transseptal Cannula (K172934)Pressure Products Medical Device Manufacturing, LLC2018-02-16
SafeSept Needle Free Transseptal Guidewire (K172893)Pressure Products Medical Device Manufacturing, LLC2017-12-21
SafeSept Transseptal Guidewire (K170671)Pressure Products Medical Device Manufacturing, LLC2017-10-20
INTRACARDIC CATHETER INTRODUCER KIT AND TRANSSEPTAL NEEDLE (K132943)Synaptic Medical Limited2014-08-29
SAFESEPT NEEDLE FREE TRANSSEPTAL TROCAR GUIDEWIRE (K130843)Oscor, Inc.2014-01-08
BRK TRANSSEPTAL NEEDLE MODEL 407200, 407201, 407205, 407206, 407207, G407208 (K122587)St Jude Medical2013-02-07

Recalls involving this device

No recalls on record reference this clearance.

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