PHORESOR II,MODEL PM900— 510(k) K982668

Substantially Equivalent

Iomed, Inc.

FDA 510(k) clearance K982668 for PHORESOR II,MODEL PM900, Substantially Equivalent on 1999-03-02. 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: 1998-07-31
Decision date: 1999-03-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, 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.