ORTHO-PLEX-REHABILITATION SYSTEM— 510(k) K920686

Name: FDA 510(k) clearance K920686
Creator: U.S. Food and Drug Administration
Published: 1992-06-11

Substantially Equivalent

Plexus Intl., Inc.

FDA 510(k) clearance K920686 for ORTHO-PLEX-REHABILITATION SYSTEM, Substantially Equivalent on 1992-06-11. Applicant: Plexus Intl., Inc.. Device class: 1.

Clearance details

Applicant: Plexus Intl., Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1992-02-14
Decision date: 1992-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

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