VISCO 360 Viscosurgical System
K-Number: K171905 · 2017-07-27
ApplicantSight Sciences, Inc.
Decision Date2017-07-27
Product CodeMRH
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
VISCO 360 Viscosurgical System is a medical device manufactured by Sight Sciences, Inc.. It received FDA 510(k) clearance on 2017-07-27 under approval number K171905. The device is classified under product code MRH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the VISCO 360 Viscosurgical System?
VISCO 360 Viscosurgical System is a medical device that received FDA 510(k) clearance on 2017-07-27. It is manufactured by Sight Sciences, Inc.. The 510(k) number is K171905.
When was VISCO 360 Viscosurgical System approved by the FDA?
VISCO 360 Viscosurgical System received FDA 510(k) clearance on 2017-07-27, under approval number K171905.
What company makes VISCO 360 Viscosurgical System?
VISCO 360 Viscosurgical System is manufactured by Sight Sciences, Inc..
What is the FDA product code for VISCO 360 Viscosurgical System?
The FDA product code for VISCO 360 Viscosurgical System is MRH.
Other Devices by Sight Sciences, Inc.
Related Devices (Code: MRH)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.