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

INTUITIVE SURGICAL DA VINCI SURGICAL SYSTEM AND ENDOSCOPIC INSTRUMENTS

K Number: K050404 · Decision Apr 21, 2005
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
176
Review Days
63

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Basic Information

Device Name
INTUITIVE SURGICAL DA VINCI SURGICAL SYSTEM AND ENDOSCOPIC INSTRUMENTS
K Number
K050404
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intuitive Surgical, Inc.
Date Received
February 17, 2005
Decision Date
April 21, 2005
Product Code
HET
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HET Laparoscope, Gynecologic (And Accessories)

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Other Clearances by Intuitive Surgical, Inc.

K Number Device Name
K253986 da Vinci Force Feedback Instruments
K253978 Universal Seal (5-12 mm)
K251739 da Vinci Surgical System (IS5000)
K253556 da Vinci SP Surgical System (SP1098); da Vinci E-200 Generator
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)
Search all 176 clearances from Intuitive Surgical, Inc. →