Modification to Intuitive Surgical Da Vinci Surgical System and Endoscopic Instruments

FDA 510(k) K043288 · Intuitive Surgical, Inc.

Substantially Equivalent

510(k) numberK043288

Submission

Device name
Modification to Intuitive Surgical Da Vinci Surgical System and Endoscopic Instruments
Applicant
Intuitive Surgical, Inc.
Sunnyvale, CA, US
Received
November 29, 2004
Decision date
March 3, 2005
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NAY – System, Surgical, Computer Controlled Instrument
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

Other 510(k)s with product code NAY

510(k)DeviceApplicantDecision
K261823da Vinci Surgical System, Model IS5000NAY · Traditional Intuitive Surgical, Inc.09/08/2026SE
K261824da Vinci Surgical System, Model IS5000NAY · Traditional Intuitive Surgical, Inc.07/31/2026SE
K260695da Vinci Firefly Imaging SystemNAY · Traditional Intuitive Surgical05/22/2026SE
K254192Senhance Ultrasonic SystemNAY · Traditional Asensus Surgical05/12/2026SE
K253986da Vinci Force Feedback InstrumentsNAY · Traditional Intuitive Surgical, Inc.03/11/2026SE
K253556da Vinci SP Surgical System (SP1098); da Vinci E-200 GeneratorNAY · Traditional Intuitive Surgical, Inc.01/16/2026SE
K251739da Vinci Surgical System (IS5000)NAY · Traditional Intuitive Surgical, Inc.01/16/2026SE
K252675da Vinci SP Surgical System (SP1098)NAY · Traditional Intuitive Surgical, Inc.12/15/2025SE
K252069da Vinci SP Surgical System (SP1098)NAY · Traditional Intuitive Surgical, Inc.12/02/2025SE
K251426da Vinci SP Surgical System (SP1098)NAY · Traditional Intuitive Surgical, Inc.10/03/2025SE

More from Intuitive Surgical, Inc.

510(k)DeviceDecision
K261823da Vinci Surgical System, Model IS5000NAY · Traditional 09/08/2026SE
K253702Intuitive Endoluminal Gastrointestinal System (IG1000)FDS · Traditional 08/07/2026SE
K261824da Vinci Surgical System, Model IS5000NAY · Traditional 07/31/2026SE
K261249Universal Seal (5-12 mm)GCJ · Traditional 07/14/2026SE
K260695da Vinci Firefly Imaging SystemNAY · Traditional 05/22/2026SE
K253986da Vinci Force Feedback InstrumentsNAY · Traditional 03/11/2026SE
K253978Universal Seal (5-12 mm)GCJ · Traditional 02/24/2026SE
K253556da Vinci SP Surgical System (SP1098); da Vinci E-200 GeneratorNAY · Traditional 01/16/2026SE
K251739da Vinci Surgical System (IS5000)NAY · Traditional 01/16/2026SE
K251763IRISegQIH · Traditional 12/16/2025SE

Questions and answers

When was Modification to Intuitive Surgical Da Vinci Surgical System and Endoscopic Instruments cleared by the FDA?

Modification to Intuitive Surgical Da Vinci Surgical System and Endoscopic Instruments (K043288) received a 510(k) decision of Substantially Equivalent on March 3, 2005, 94 days after the submission was received.

What is the product code of K043288?

The FDA product code is NAY – System, Surgical, Computer Controlled Instrument, a Class II (moderate risk) device regulated under 21 CFR 876.1500.