ADR-2000 AMBULATORY DATA RECORDING SYSTEM— 510(k) K880977

Name: FDA 510(k) clearance K880977
Creator: U.S. Food and Drug Administration
Published: 1988-04-13

Substantially Equivalent

Aaron Laboratories, Inc.

FDA 510(k) clearance K880977 for ADR-2000 AMBULATORY DATA RECORDING SYSTEM, Substantially Equivalent on 1988-04-13. Applicant: Aaron Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Aaron Laboratories, Inc.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1988-03-08
Decision date: 1988-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IKN

view all

K172743 — Natus VikingQuest2017-12-19
K163150 — ViMove22017-07-14
K162383 — Cadwell Sierra Summit, Cadwell Sierra Ascent2017-03-01
K142494 — ViMove2015-05-28
K131094 — VIMOVE2014-07-11

More clearances from Aaron Laboratories, Inc.

view all

K880976 — AL-200B MUSCLE ACTIVITY INTEGRATOR1988-04-13

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