Atlas FDA

SCANLAN ENDARSECTOR

FDA 510(k) clearance K841521 · decided 1984-08-03

Clearance details

K-number
K841521
Device name
SCANLAN ENDARSECTOR
Applicant
Scanlan Intl., Inc.
Decision
Substantially Equivalent
Date received
1984-04-12
Decision date
1984-08-03
Days to decision
113 days
Clearance type
Traditional
Product code
DWX
Device class
2
Regulation number
870.4875
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Mchenry, IL, 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
MOLLRING MULTITASC (K121415)LeMaitre Vascular, Inc.2012-09-05
ENDOHELIX ENDARTERECTOMY DEVICE (K032105)Endarx, Inc.2003-10-30
CARBODISSECTING ENDOSCOPE (K020925)Endo Surgical Devices, Inc.2003-04-29
VASCULAR ARCHITECTS PERISCOPE DEVICE (K003719)Vascular Architects, Inc.2001-02-28
MOLLRING CUTTER (K950813)Cardio Vascular Concepts, Inc.1995-07-25
EXTERNAL VEIN STRIPPER (K933498)Applied Medical Resources1994-03-23
INTRALUMINAL ARTERY STRIPPER (K913803)Omni-Tract Surgical, Div. Minn. Scientific, Inc.1992-04-24
MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE (K911099)Pilling Co.1991-06-25
TRANSLUMINAL ENDARTERECTOMY DEVICE (K904944)Baxter Healthcare Corp1990-12-17
OLYMPUS VALVULOTOME W/DETACHABLE TIP (K895878)Olympus Corp.1990-01-02
OLYMPUS VALVULOTOME W/FIXED TIP (K894496)Olympus Corp.1989-10-12
PERIPHERAL ATHERECTOMY SYSTEM (K890515)Intensive Technology, Inc.1989-05-23

Recalls involving this device

No recalls on record reference this clearance.