PHOTRON NEUROVISUAL STIMULATOR(MODIFICATION)— 510(k) K853812

Name: FDA 510(k) clearance K853812
Creator: U.S. Food and Drug Administration
Published: 1985-11-01

Substantially Equivalent

Biosan Laboratories, Inc.

FDA 510(k) clearance K853812 for PHOTRON NEUROVISUAL STIMULATOR(MODIFICATION), Substantially Equivalent on 1985-11-01. Applicant: Biosan Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Biosan Laboratories, Inc.
Product code: Code HLX
Device class: Class 2
Regulation: 21 CFR 886.1630
Advisory panel: Ophthalmic
Date received: 1985-09-12
Decision date: 1985-11-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Rafael, CA, US

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