DICON GLAUCOMA DIAG. CENTER 2000 SERIES— 510(k) K832142

Substantially Equivalent

CooperVision, Inc.

FDA 510(k) clearance K832142 for DICON GLAUCOMA DIAG. CENTER 2000 SERIES, Substantially Equivalent on 1983-08-01. Applicant: CooperVision, Inc..

Clearance details

Applicant: CooperVision, Inc.
Product code: Code HPT
Advisory panel: Ophthalmic
Date received: 1983-07-05
Decision date: 1983-08-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Southampton, GB

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.