LATERAL FLEXION MACHINE— 510(k) K940455

Name: FDA 510(k) clearance K940455
Creator: U.S. Food and Drug Administration
Published: 1995-01-12

Substantially Equivalent for Some Indications

Rehab, Inc.

FDA 510(k) clearance K940455 for LATERAL FLEXION MACHINE, Substantially Equivalent for Some Indications on 1995-01-12. Applicant: Rehab, Inc.. Device class: 1.

Clearance details

Applicant: Rehab, Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1994-02-01
Decision date: 1995-01-12
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Knoxville, TN, US

Download summary PDF View on FDA.gov ↗

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