PHORESOR II (TM), MODEL PM700— 510(k) K872040

Name: FDA 510(k) clearance K872040
Creator: U.S. Food and Drug Administration
Published: 1987-08-04

Substantially Equivalent

Motion Control, Inc.

FDA 510(k) clearance K872040 for PHORESOR II (TM), MODEL PM700, Substantially Equivalent on 1987-08-04. Applicant: Motion Control, Inc.. Device class: 2.

Clearance details

Applicant: Motion Control, Inc.
Product code: Code EGJ
Device class: Class 2
Regulation: 21 CFR 890.5525
Advisory panel: Physical Medicine
Date received: 1987-05-27
Decision date: 1987-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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