510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K896444Unknown

Iontophoresis Device - Electrode Rh 800

Iomed, Inc., Salt Lake City UT / Traditional, Unknown
FDA source (opens on fda.gov)

K896444 is the FDA 510(k) clearance record for IONTOPHORESIS DEVICE - ELECTRODE RH 800, a class II device, cleared for Iomed, Inc. on under FDA product code EGJ (Device, Iontophoresis, Other Uses). FDA records list 17 510(k) clearances for Iomed, Inc., from to . As of , FDA records show no recalls naming K896444.

Clearance record

Decision date
Received
(182 days to decision)
Product code
EGJ Device, Iontophoresis, Other Uses
Regulation
21 CFR 890.5525
Device class
Class II
Review panel
Physical Medicine
Applicant
Iomed, Inc. 2471 E. Shadow Wood Cir., Salt Lake City UT
Third party review
No

Clearances, product code EGJ

Trailing 12 months

FDA records hold no clearances under product code EGJ in the trailing twelve months.

FDA records show no clearances under product code EGJ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EGJ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260