3D VASCULAR RECORDER— 510(k) K883908

Substantially Equivalent

D. E. Hokanson, Inc.

FDA 510(k) clearance K883908 for 3D VASCULAR RECORDER, Substantially Equivalent on 1988-10-28. Applicant: D. E. Hokanson, Inc.. Device class: 2.

Clearance details

Applicant: D. E. Hokanson, Inc.
Product code: Code JOM
Device class: Class 2
Regulation: 21 CFR 870.2780
Advisory panel: Cardiovascular
Date received: 1988-09-15
Decision date: 1988-10-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Issaquah, WA, US

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