Home / 510(k) Clearances / K171905

510(k) K171905

VISCO 360 Viscosurgical System by Sight Sciences, Inc. — Product Code MRH

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 27, 2017
Date Received
June 26, 2017
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pump, Infusion, Ophthalmic
Device Class
Class II
Regulation Number
880.5725
Review Panel
OP
Submission Type

Other clearances by Sight Sciences, Inc.

  • K242786 — TearCare MGX System (April 15, 2025)
  • K231084 — TearCare MGX System (December 27, 2023)
  • K232214 — OMNI Surgical System (August 25, 2023)
  • K213045 — TearCare System (December 21, 2021)
  • K202678 — OMNI Surgical System (March 1, 2021)
  • K201953 — OMNI PLUS Surgical System (August 11, 2020)
  • K173332 — OMNI Surgical System (December 21, 2017)
  • K143205 — Viscoelastic Injector (December 5, 2014)
  • K132494 — VISCOELASTIC INJECTOR (October 22, 2013)

Other clearances for product code MRH

  • K243503 — VIA360™ Surgical System (February 14, 2025)
  • K232214 — OMNI Surgical System (August 25, 2023)
  • K213173 — TrabEx Pro (June 8, 2022)
  • K212797 — iPrime Viscodelivery System (January 6, 2022)
  • K211680 — Streamline Surgical System (October 8, 2021)
  • K202678 — OMNI Surgical System (March 1, 2021)
  • K201953 — OMNI PLUS Surgical System (August 11, 2020)
  • K173332 — OMNI Surgical System (December 21, 2017)
  • K143205 — Viscoelastic Injector (December 5, 2014)
  • K132494 — VISCOELASTIC INJECTOR (October 22, 2013)