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

G-CATH TISSUE ANCHOR DELIVERY CATHETER, MODELS 205302, 205333

K Number: K100251 · Decision Feb 17, 2010
Classifications
1
FEI Numbers
233
Registration Numbers
233
Same Product Code
166
Applicant Total
11
Review Days
20

Basic Information

Device Name
G-CATH TISSUE ANCHOR DELIVERY CATHETER, MODELS 205302, 205333
K Number
K100251
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.5000
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
USGI MEDICAL
Date Received
January 28, 2010
Decision Date
February 17, 2010
Product Code
GAT
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GAT Suture, Nonabsorbable, Synthetic, Polyethylene

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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
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