RH-806/GS MODEL TRANSQ(R)2— 510(k) K932620

Substantially Equivalent

Iomed, Inc.

FDA 510(k) clearance K932620 for RH-806/GS MODEL TRANSQ(R)2, 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: 1993-06-01
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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Data sourced from openFDA. This site is unofficial and independent of the FDA.