PainShield MD PLUS— 510(k) K221210

Substantially Equivalent

Nanovibronix, Inc.

FDA 510(k) clearance K221210 for PainShield MD PLUS, Substantially Equivalent on 2022-11-23. Applicant: Nanovibronix, Inc.. Device class: 2.

Clearance details

Applicant: Nanovibronix, Inc.
Product code: Code PFW
Device class: Class 2
Regulation: 21 CFR 890.5300
Advisory panel: Physical Medicine
Date received: 2022-04-27
Decision date: 2022-11-23
Decision: Substantially Equivalent
Clearance type: Special
Location: Elmsford, NY, 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.