FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇪 Ireland

EndoFLIP System

K Number: K183072 · Decision Feb 15, 2019
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
68
Applicant Total
12
Review Days
102

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Basic Information

Device Name
EndoFLIP System
K Number
K183072
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1725
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Crospon, Ltd.
Date Received
November 5, 2018
Decision Date
February 15, 2019
Product Code
FFX
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
FFX System, Gastrointestinal Motility (Electrical)

Similar 510(k) Clearances

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

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Other Clearances by Crospon, Ltd.

K Number Device Name
K172128 EsoFLIP® ES-310 Balloon Catheter
K170833 EndoFLIP® System with FLIP Topography module
K160725 EndoFLIP
K142000 ESOFLIP ES
K132337 ESOFLIP BALLOON DILATION CATHETER
K130906 ENDOFLIP CATHETER
K120997 BAROSTAT SOFTWARE OPTION
K110531 ENDOFLIP ECD
K110529 ENDOFLIP GASTRIC TUBE
K102214 ENDO FLIP
Search all 12 clearances from Crospon, Ltd. →