CWAS 1000— 510(k) K033452

Substantially Equivalent

Fasstech

FDA 510(k) clearance K033452 for CWAS 1000, Substantially Equivalent on 2003-11-28. Applicant: Fasstech. Device class: 2.

Clearance details

Applicant: Fasstech
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 2003-10-30
Decision date: 2003-11-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Billerica, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IKN

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K142494 — ViMove2015-05-28
K131094 — VIMOVE2014-07-11

More clearances from Fasstech

K063447 — INSIGHT DISCOVERY2007-08-16
K023209 — INSIGHT MILLENNIUM III2003-10-10
K011964 — INSIGHT MILLENNIUM PLUS2001-09-20
K011983 — INSIGHT GENESIS2001-08-30
K990778 — INSIGHT MILLENNIUM1999-06-03

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