NEOLENS PRESCRIPTION SPECTACLE LENS— 510(k) K882814

Substantially Equivalent

Neolens, Inc.

FDA 510(k) clearance K882814 for NEOLENS PRESCRIPTION SPECTACLE LENS, Substantially Equivalent on 1988-07-29. Applicant: Neolens, Inc..

Clearance details

Applicant: Neolens, Inc.
Product code: Code HQG
Advisory panel: Ophthalmic
Date received: 1988-07-08
Decision date: 1988-07-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

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