MESODERM— 510(k) K061849

Substantially Equivalent

Aa Advanced Technology, Inc.

FDA 510(k) clearance K061849 for MESODERM, Substantially Equivalent on 2007-04-30. Applicant: Aa Advanced Technology, Inc.. Device class: 2.

Clearance details

Applicant: Aa Advanced Technology, Inc.
Product code: Code EGJ
Device class: Class 2
Regulation: 21 CFR 890.5525
Advisory panel: Physical Medicine
Date received: 2006-06-30
Decision date: 2007-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Crofton, MD, 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

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