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

G-PROX EZ ENDOSCOPIC GRASPER

K Number: K103688 · Decision Jan 14, 2011
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
73
Applicant Total
11
Review Days
28

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Basic Information

Device Name
G-PROX EZ ENDOSCOPIC GRASPER
K Number
K103688
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Usgi Medical
Date Received
December 17, 2010
Decision Date
January 14, 2011
Product Code
OCZ
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
OCZ Endoscopic Grasping/Cutting Instrument, Non-Powered

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Other Clearances by Usgi Medical

K Number Device Name
K102931 G-CINCH SUTURE GRASPER
K102916 G-CATH TISSUE ANCHOR DELIVERY CATHETER
K100251 G-CATH TISSUE ANCHOR DELIVERY CATHETER, MODELS 205302, 205333
K093018 G-PROX ENDOSCOPIC GRASPER, MODEL 205333
K072405 USGI TRANSPORT ENDOSCOPIC ACCESS DEVICE
K061276 G-PROX ENDOSCOPIC GRASPER
K061268 G-LIX TISSUE GRASPER
K061216 USGI TRANSPORT ENDOSCOPIC GUIDE
K051919 MODIFICATION TO: USGI SHAPELOCK ENDOSCOPIC GUIDE
K050253 USGI SHAPELOCK ENDOSCOPIC GUIDE
Search all 11 clearances from Usgi Medical →