FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

WALLSTENT ESOPHAGEAL PROSTHESIS (DOUBLE)

K Number: K940396 · Decision Oct 3, 1994
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
58
Applicant Total
35
Review Days
249

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Basic Information

Device Name
WALLSTENT ESOPHAGEAL PROSTHESIS (DOUBLE)
K Number
K940396
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3610
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Boston Scientific Scimed, Inc.
Date Received
January 27, 1994
Decision Date
October 3, 1994
Product Code
ESW
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ESW Prosthesis, Esophageal

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Other Clearances by Boston Scientific Scimed, Inc.

K Number Device Name
K041727 MODIFICATION TO ATLANTIS PV IMAGING CATHETER, MODEL 36456
K030617 PT2 GUIDE WIRE AND ADDWIRE EXTENSION WIRE
K024048 MODIFICATION TO BOSTON SCIENTIFIC EXPRESS BILIARY LD PREMOUNTED STENT SYSTEM
K021735 BOSTON SCIENTIFIC ULTRA-SOFT SV BALLOON DILATATION CATHETER
K021901 WALLGRAFT TRACHEOBRONCHIAL ENDOPROTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM
K012822 MODIFICIATION TO: BILIARY WALLSTENT ENDOPROSTHEIS WITH MONORAIL DELIVERY SYSTEM, MODEL 71-XXX
K012216 NIROYAL BILIARY PREMOUNTED STENT SYSTEM
K000743 BOSTON SCIENTIFIC SCIMED ATLANTIS CORONARY IMAGING CATHETER, MODEL C4020
K000001 WALLGRAFT TRACHEOBRONCHIAL ENDOPROSTHESIS AND UNISTEP DELIVERY SYSTEM
K000956 MODIFICATION TO SCIMED 6F IMPULSE ANGIOGRAPHIC CATHATERS
Search all 35 clearances from Boston Scientific Scimed, Inc. →