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DERMOSONIC NON-INVASIVE SUBDERMAL THERAPY SYSTEM

K052934 Class II Traditional
Decision Date
2006-06-12
Sponsor / Applicant
S.O.R. Internacional, S.A.

Technical Specification

510(k) Submission ID K052934
Product Code IMI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5300
Decision Date 2006-06-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DERMOSONIC NON-INVASIVE SUBDERMAL THERAPY SYSTEM received FDA 510(k) clearance under submission number K052934, sponsored by S.O.R. Internacional, S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2006-06-12.

Classification & Regulation

This clearance is catalogued under FDA product code IMI and 21 CFR 890.5300, within the Physical Medicine review panel as a Class II device.