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

ENDOSCOPE STERILIZATION TRAY

K Number: K133942 · Decision Aug 1, 2014
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
279
Applicant Total
17
Review Days
221

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Basic Information

Device Name
ENDOSCOPE STERILIZATION TRAY
K Number
K133942
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intuitive Surgical
Date Received
December 23, 2013
Decision Date
August 1, 2014
Product Code
KCT
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

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Other Clearances by Intuitive Surgical

K Number Device Name
K260695 da Vinci Firefly Imaging System
K241635 da Vinci E-200 Electrosurgical Generator
K241621 Da Vinci Monopolar and Bipolar Adapters (378896)
K240723 da Vinci Xi Surgical System (IS4000); da Vinci X Surgical System (IS4200)
K231212 da Vinci E-200 Electrosurgical Generator
K223039 da Vinci E-200 Electrosurgical Generator
K192803 da Vinci Xi Surgical System, da Vinci X Surgical System
K191529 da Vinci Xi Surgical System, da Vinci X Surgical System
K191736 da Vinci X/Xi 8mm Endoscope Plus, 0, da Vinci X/Xi 8mm Endoscope Plus, 30
K182643 IRIS 1.0 System
Search all 17 clearances from Intuitive Surgical →