PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH— 510(k) K832374

Name: FDA 510(k) clearance K832374
Creator: U.S. Food and Drug Administration
Published: 1983-12-01

Substantially Equivalent

Sonicaid, Inc.

FDA 510(k) clearance K832374 for PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH, Substantially Equivalent on 1983-12-01. Applicant: Sonicaid, Inc.. Device class: 2.

Clearance details

Applicant: Sonicaid, Inc.
Product code: Code JOM
Device class: Class 2
Regulation: 21 CFR 870.2780
Advisory panel: Cardiovascular
Date received: 1983-07-18
Decision date: 1983-12-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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