MD-2 IONTOPHORESIS UNIT— 510(k) K895365

Unknown

R. A. Fischer Co. Corp.

FDA 510(k) clearance K895365 for MD-2 IONTOPHORESIS UNIT, Unknown on 1990-06-26. Applicant: R. A. Fischer Co. Corp.. Device class: 2.

Clearance details

Applicant: R. A. Fischer Co. Corp.
Product code: Code EGJ
Device class: Class 2
Regulation: 21 CFR 890.5525
Advisory panel: Physical Medicine
Date received: 1989-08-28
Decision date: 1990-06-26
Decision: Unknown
Clearance type: Traditional
Location: Glendale, CA, 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 R. A. Fischer Co. Corp.

K964208 — MD-1A GALVANIC UNIT1997-04-30
K954031 — COMPU-BLEND EPILATOR1996-01-05
K893389 — MODEL SE-5 EPILATOR1989-06-05
K884079 — MODEL CBX EPILATOR1988-10-04
K871372 — CB-7 ELECTRONIC EPILATOR1987-04-28

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