OMNI PLUS Surgical System— 510(k) K201953

Substantially Equivalent

Sight Sciences, Inc.

FDA 510(k) clearance K201953 for OMNI PLUS Surgical System, Substantially Equivalent on 2020-08-11. Applicant: Sight Sciences, Inc.. Device class: 2.

Clearance details

Applicant: Sight Sciences, Inc.
Product code: Code MRH
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 2020-07-14
Decision date: 2020-08-11
Decision: Substantially Equivalent
Clearance type: Special
Location: Menlo Park, CA, US

Download summary PDF View on FDA.gov ↗

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