NICOLET VIKING II SYSTEM— 510(k) K890495

Name: FDA 510(k) clearance K890495
Creator: U.S. Food and Drug Administration
Published: 1989-03-16

Substantially Equivalent

Nicolet Instrument Corp.

FDA 510(k) clearance K890495 for NICOLET VIKING II SYSTEM, Substantially Equivalent on 1989-03-16. Applicant: Nicolet Instrument Corp.. Device class: 2.

Clearance details

Applicant: Nicolet Instrument Corp.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1989-02-01
Decision date: 1989-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Madison, WI, 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 Nicolet Instrument Corp.

view all

K921138 — NICOLET ULTRASOM ACQUISITION STATION1993-05-14
K923315 — NICOLET ARK SYSTEM1992-11-23
K921927 — NICOLET VOYAGEUR1992-11-05
K915652 — NICOLET PORATBLE SPIRIT SYSTEM1992-02-07
K905632 — NICOLET MAPLELEAF SYSTEM1991-06-07

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