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FDA 510(k)

DERMOSONIC NON-INVASIVE SUBDERMAL THERAPY SYSTEM

K-Number: K052934 · 2006-06-12

ApplicantS.O.R. Internacional, S.A.
Decision Date2006-06-12
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DERMOSONIC NON-INVASIVE SUBDERMAL THERAPY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is S.O.R. Internacional, S.A.. It received FDA 510(k) clearance on 2006-06-12 under 510(k) number K052934. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMOSONIC NON-INVASIVE SUBDERMAL THERAPY SYSTEM?

DERMOSONIC NON-INVASIVE SUBDERMAL THERAPY SYSTEM is a medical device that received FDA 510(k) clearance on 2006-06-12. The listed applicant is S.O.R. Internacional, S.A.. The 510(k) number is K052934.

When did DERMOSONIC NON-INVASIVE SUBDERMAL THERAPY SYSTEM receive FDA 510(k) clearance?

DERMOSONIC NON-INVASIVE SUBDERMAL THERAPY SYSTEM received FDA 510(k) clearance on 2006-06-12, under 510(k) number K052934.

Who is the listed applicant for DERMOSONIC NON-INVASIVE SUBDERMAL THERAPY SYSTEM?

The FDA 510(k) record lists S.O.R. Internacional, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DERMOSONIC NON-INVASIVE SUBDERMAL THERAPY SYSTEM?

The FDA product code for DERMOSONIC NON-INVASIVE SUBDERMAL THERAPY SYSTEM is IMI.

Related Clinical Trials

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Related Devices (Code: IMI)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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