FLEXXR* CPM SYSTEM— 510(k) K834203

Substantially Equivalent

Qarex Laboratories, Inc.

FDA 510(k) clearance K834203 for FLEXXR* CPM SYSTEM, Substantially Equivalent on 1984-01-30. Applicant: Qarex Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Qarex Laboratories, Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1983-12-05
Decision date: 1984-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.