RH-801, MODEL TRANSQ— 510(k) K925806

Substantially Equivalent

Iomed, Inc.

FDA 510(k) clearance K925806 for RH-801, MODEL TRANSQ, Substantially Equivalent on 1994-07-14. 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: 1992-11-16
Decision date: 1994-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EGJ

K242041 — STOPWET iontophoresis apparatus (SW01)2025-04-01
K241267 — Hidroxa SE302024-10-17
K232020 — Iontophoresis Electrodes2023-10-16
K192749 — Dermadry2020-02-10
K191436 — Saalio2019-10-18

More clearances from Iomed, Inc.

K063465 — CHAMPION IONTOPHORETIC DRUG DELIVERY DEVICE2007-02-28
K060236 — MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE2006-03-31
K033192 — RH-9502003-12-22
K031115 — RH-9002003-07-10
K001522 — TRANSQ32000-10-18

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