OCULAR CEREBRAL VASCULAR MONITOR— 510(k) K772130

Substantially Equivalent

Digilab, Inc.

FDA 510(k) clearance K772130 for OCULAR CEREBRAL VASCULAR MONITOR, Substantially Equivalent on 1977-11-28. Applicant: Digilab, Inc.. Device class: 2.

Clearance details

Applicant: Digilab, Inc.
Product code: Code HKY
Device class: Class 2
Regulation: 21 CFR 886.1930
Advisory panel: Ophthalmic
Date received: 1977-11-11
Decision date: 1977-11-28
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.