SUNETICS CLINICAL BIO-STIMULATION LASER— 510(k) K132646

Substantially Equivalent

Sunetics International Marketing Group, LLC

FDA 510(k) clearance K132646 for SUNETICS CLINICAL BIO-STIMULATION LASER, Substantially Equivalent on 2013-12-20. Applicant: Sunetics International Marketing Group, LLC. Device class: 2.

Clearance details

Applicant
Sunetics International Marketing Group, LLC
Product code
Code OAP
Device class
Class 2
Regulation
21 CFR 890.5500
Advisory panel
Physical Medicine
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Rockwall, TX, US
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