MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFOR— 510(k) K850877

Name: FDA 510(k) clearance K850877
Creator: U.S. Food and Drug Administration
Published: 1985-06-12

Substantially Equivalent

Ketronic, Inc.

FDA 510(k) clearance K850877 for MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFOR, Substantially Equivalent on 1985-06-12. Applicant: Ketronic, Inc.. Device class: 2.

Clearance details

Applicant: Ketronic, Inc.
Product code: Code ILK
Device class: Class 2
Regulation: 21 CFR 890.5150
Advisory panel: Physical Medicine
Date received: 1985-03-01
Decision date: 1985-06-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: The Netherlands, NL

Download summary PDF View on FDA.gov ↗

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