MINI VIBRATOR— 510(k) K920487

Substantially Equivalent

Alimed, Inc.

FDA 510(k) clearance K920487 for MINI VIBRATOR, Substantially Equivalent on 1992-02-18. Applicant: Alimed, Inc.. Device class: 1.

Clearance details

Applicant: Alimed, Inc.
Product code: Code IRO
Device class: Class 1
Regulation: 21 CFR 890.5975
Advisory panel: Physical Medicine
Date received: 1992-01-30
Decision date: 1992-02-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dedham, MA, US

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