BEMER Therapy Systems, BEMER Classic Set, BEMER Pro-Set— 510(k) K210174

Name: FDA 510(k) clearance K210174
Creator: U.S. Food and Drug Administration
Published: 2021-02-04

Substantially Equivalent

Bemer Int AG

FDA 510(k) clearance K210174 for BEMER Therapy Systems, BEMER Classic Set, BEMER Pro-Set, Substantially Equivalent on 2021-02-04. Applicant: Bemer Int AG. Device class: 2.

Clearance details

Applicant: Bemer Int AG
Product code: Code NGX
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2021-01-22
Decision date: 2021-02-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Triesen, LI

Download summary PDF View on FDA.gov ↗

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More clearances from Bemer Int AG

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K223919 — B.Light Clear Evo and B.Light Restore Evo2023-09-23
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K151834 — BEMER Classic Set, BEMER Pro-Set2017-02-22

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