PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAM— 510(k) K881358

Name: FDA 510(k) clearance K881358
Creator: U.S. Food and Drug Administration
Published: 1988-06-27

Substantially Equivalent

Neuroscientific Corp.

FDA 510(k) clearance K881358 for PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAM, Substantially Equivalent on 1988-06-27. Applicant: Neuroscientific Corp.. Device class: 1.

Clearance details

Applicant: Neuroscientific Corp.
Product code: Code HOX
Device class: Class 1
Regulation: 21 CFR 886.1150
Advisory panel: Ophthalmic
Date received: 1988-03-31
Decision date: 1988-06-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Farmingdale, NY, US

Download summary PDF View on FDA.gov ↗

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