AUTO PERIOMETER 3000— 510(k) K822580

Substantially Equivalent

Dicon, Inc.

FDA 510(k) clearance K822580 for AUTO PERIOMETER 3000, Substantially Equivalent on 1982-09-30. Applicant: Dicon, Inc.. Device class: 1.

Clearance details

Applicant: Dicon, Inc.
Product code: Code HPT
Device class: Class 1
Regulation: 21 CFR 886.1605
Advisory panel: Ophthalmic
Date received: 1982-08-25
Decision date: 1982-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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