Atlas FDA

DA VINCI FIREFLY IMAGING SYSTEM

FDA 510(k) clearance K141077 · decided 2014-08-12

Clearance details

K-number
K141077
Device name
DA VINCI FIREFLY IMAGING SYSTEM
Applicant
Intuitive Surgical, Inc.
Decision
Substantially Equivalent
Date received
2014-04-25
Decision date
2014-08-12
Days to decision
109 days
Clearance type
Traditional
Product code
NAY
Device class
2
Regulation number
876.1500
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Sunnyvale, CA, US
Third-party review
No
Expedited review
No

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da Vinci SP Surgical System (SP1098) (K252069)Intuitive Surgical, Inc.2025-12-02
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Recalls involving this device

RecordFirmDate
Fluorescence Imaging Procedure Kits used with the da Vinci Si and Xi Surgical Systems; Mod recall (Z-2782-2015)Intuitive Surgical, Inc.2015-09-17
Fluorescence Imaging Procedure Kit, designed for use with Firefly Fluorescence Imaging for recall (Z-0835-2015)Intuitive Surgical, Inc.2014-12-19