CERVICAL PASSIVE MOTION— 510(k) K921323

Name: FDA 510(k) clearance K921323
Creator: U.S. Food and Drug Administration
Published: 1992-06-03

Substantially Equivalent

Rehabilitative Resources, Inc.

FDA 510(k) clearance K921323 for CERVICAL PASSIVE MOTION, Substantially Equivalent on 1992-06-03. Applicant: Rehabilitative Resources, Inc.. Device class: 1.

Clearance details

Applicant: Rehabilitative Resources, Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1992-03-18
Decision date: 1992-06-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oliver Springs, TN, US

Download summary PDF View on FDA.gov ↗

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