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

ESOFLIP BALLOON DILATION CATHETER

K Number: K132337 · Decision Oct 7, 2013
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
2
Applicant Total
12
Review Days
73

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Basic Information

Device Name
ESOFLIP BALLOON DILATION CATHETER
K Number
K132337
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Crospon, Ltd.
Date Received
July 26, 2013
Decision Date
October 7, 2013
Product Code
PID
Advisory Committee
Gastroenterology, Urology
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
PID Esophageal Dilator Balloon With Or Without Electrode Sensors

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PID), ordered by most recent decision date.

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Other Clearances by Crospon, Ltd.

K Number Device Name
K183072 EndoFLIP System
K172128 EsoFLIP® ES-310 Balloon Catheter
K170833 EndoFLIP® System with FLIP Topography module
K160725 EndoFLIP
K142000 ESOFLIP ES
K130906 ENDOFLIP CATHETER
K120997 BAROSTAT SOFTWARE OPTION
K110531 ENDOFLIP ECD
K110529 ENDOFLIP GASTRIC TUBE
K102214 ENDO FLIP
Search all 12 clearances from Crospon, Ltd. →