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

CLEARPATH

K Number: K091305 · Decision Oct 23, 2009
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
111
Applicant Total
5
Review Days
172

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Basic Information

Device Name
CLEARPATH
K Number
K091305
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Easyglide , Ltd.
Date Received
May 4, 2009
Decision Date
October 23, 2009
Product Code
FDF
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
FDF Colonoscope And Accessories, Flexible/Rigid

Similar 510(k) Clearances

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

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Other Clearances by Easyglide , Ltd.

K Number Device Name
K113166 CLEARPATH UPPER GI
K113050 CLEARPATH LOWER GI
K101094 CLEARJET
K093779 CLEARPATH UGI