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

INTUITIVE SURGICAL ENDOWRIST ENDOSCOPIC INSTRUMENT FAMILY

K Number: K013416 · Decision Jan 10, 2002
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
176
Review Days
87

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Basic Information

Device Name
INTUITIVE SURGICAL ENDOWRIST ENDOSCOPIC INSTRUMENT FAMILY
K Number
K013416
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intuitive Surgical, Inc.
Date Received
October 15, 2001
Decision Date
January 10, 2002
Product Code
GEI
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

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K251763 IRISeg
K252675 da Vinci SP Surgical System (SP1098)
K252069 da Vinci SP Surgical System (SP1098)
K251426 da Vinci SP Surgical System (SP1098)
K252045 Ion Endoluminal System (IF1000)
K251817 da Vinci SP Surgical System (SP1098)
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