TREDBAND TYPE I, IT, II & III - TREADMILLS— 510(k) K850871

Name: FDA 510(k) clearance K850871
Creator: U.S. Food and Drug Administration
Published: 1985-06-05

Substantially Equivalent

Ketronic, Inc.

FDA 510(k) clearance K850871 for TREDBAND TYPE I, IT, II & III - TREADMILLS, Substantially Equivalent on 1985-06-05. Applicant: Ketronic, Inc.. Device class: 1.

Clearance details

Applicant: Ketronic, Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1985-03-01
Decision date: 1985-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: The Netherlands, NL

Download summary PDF View on FDA.gov ↗

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