PHORESOR II, MODEL PM900— 510(k) K974855

Name: FDA 510(k) clearance K974855
Creator: U.S. Food and Drug Administration
Published: 1998-03-27

Substantially Equivalent for Some Indications

Iomed, Inc.

FDA 510(k) clearance K974855 for PHORESOR II, MODEL PM900, Substantially Equivalent for Some Indications on 1998-03-27. Applicant: Iomed, Inc.. Device class: 2.

Clearance details

Applicant: Iomed, Inc.
Product code: Code KTB
Device class: Class 2
Regulation: 21 CFR 890.5525
Advisory panel: Physical Medicine
Date received: 1997-12-29
Decision date: 1998-03-27
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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