EC 5R PLETHYSMOGRAPH— 510(k) K932812

Substantially Equivalent

D. E. Hokanson, Inc.

FDA 510(k) clearance K932812 for EC 5R PLETHYSMOGRAPH, Substantially Equivalent on 1994-01-13. Applicant: D. E. Hokanson, Inc.. Device class: 2.

Clearance details

Applicant: D. E. Hokanson, Inc.
Product code: Code JEH
Device class: Class 2
Regulation: 21 CFR 868.1760
Advisory panel: Anesthesiology
Date received: 1993-06-09
Decision date: 1994-01-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bellevue, WA, 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.