RH-900— 510(k) K031115

Substantially Equivalent

Iomed, Inc.

FDA 510(k) clearance K031115 for RH-900, Substantially Equivalent on 2003-07-10. 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: 2003-04-08
Decision date: 2003-07-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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K982668 — PHORESOR II,MODEL PM9001999-03-02
K974855 — PHORESOR II, MODEL PM9001998-03-27

Data sourced from openFDA. This site is unofficial and independent of the FDA.