ACTIC 2002— 510(k) K946169

Substantially Equivalent

North Atlantic Rehabilitation, Inc.

FDA 510(k) clearance K946169 for ACTIC 2002, Substantially Equivalent on 1995-06-15. Applicant: North Atlantic Rehabilitation, Inc.. Device class: 1.

Clearance details

Applicant: North Atlantic Rehabilitation, Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1994-12-19
Decision date: 1995-06-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Bend, WI, US

Download summary PDF View on FDA.gov ↗

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