PHORESOR II AUTO, MODEL PM800 MODIFICATION— 510(k) K934335

Name: FDA 510(k) clearance K934335
Creator: U.S. Food and Drug Administration
Published: 1994-07-26

Substantially Equivalent

Iomed, Inc.

FDA 510(k) clearance K934335 for PHORESOR II AUTO, MODEL PM800 MODIFICATION, Substantially Equivalent on 1994-07-26. Applicant: Iomed, Inc.. Device class: 2.

Clearance details

Applicant: Iomed, Inc.
Product code: Code EGJ
Device class: Class 2
Regulation: 21 CFR 890.5525
Advisory panel: Physical Medicine
Date received: 1993-09-07
Decision date: 1994-07-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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