AMES THERAPY DEVICE— 510(k) K123746

Substantially Equivalent

Ames Technology, Inc.

FDA 510(k) clearance K123746 for AMES THERAPY DEVICE, Substantially Equivalent on 2013-05-24. Applicant: Ames Technology, Inc.. Device class: 2.

Clearance details

Applicant: Ames Technology, Inc.
Product code: Code IKK
Device class: Class 2
Regulation: 21 CFR 890.1925
Advisory panel: Physical Medicine
Date received: 2012-12-06
Decision date: 2013-05-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eugene, OR, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IKK

K952090 — HUMAC SYSTEM1995-12-11
K951770 — BIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3AP1995-11-16
K951916 — CC RIDER, MODEL ME1801995-10-04
K950095 — CYBEX 7701995-06-21
K942229 — MOTIVATOR FTR 20001995-02-27

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