AUTOMATIC OBJECTIVE REFRACTOR 2000— 510(k) K820877

Substantially Equivalent

Dicon, Inc.

FDA 510(k) clearance K820877 for AUTOMATIC OBJECTIVE REFRACTOR 2000, Substantially Equivalent on 1982-06-25. Applicant: Dicon, Inc.. Device class: 1.

Clearance details

Applicant: Dicon, Inc.
Product code: Code HKO
Device class: Class 1
Regulation: 21 CFR 886.1760
Advisory panel: Ophthalmic
Date received: 1982-03-30
Decision date: 1982-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Dicon, Inc.

K822580 — AUTO PERIOMETER 30001982-09-30
K811346 — DICON AUTO PERIMETER 2001981-08-20
K811347 — DICON AUTO PERIMETER 20001981-08-20

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