REHABOT-YM— 510(k) K890838

Substantially Equivalent

Imex Health, Inc.

FDA 510(k) clearance K890838 for REHABOT-YM, Substantially Equivalent on 1989-03-23. Applicant: Imex Health, Inc.. Device class: 1.

Clearance details

Applicant: Imex Health, Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1989-02-21
Decision date: 1989-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.