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FDA 510(k)

LIPOSONIX SYSTEM, MODEL 1 P00XXXX

K-Number: K100874 · 2011-08-19

ApplicantMedicis Technologies Corporation
Decision Date2011-08-19
Product CodeOHV
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIPOSONIX SYSTEM, MODEL 1 P00XXXX is the device name listed in this FDA 510(k) record. The listed applicant is Medicis Technologies Corporation. It received FDA 510(k) clearance on 2011-08-19 under 510(k) number K100874. The device is classified under product code OHV. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIPOSONIX SYSTEM, MODEL 1 P00XXXX?

LIPOSONIX SYSTEM, MODEL 1 P00XXXX is a medical device that received FDA 510(k) clearance on 2011-08-19. The listed applicant is Medicis Technologies Corporation. The 510(k) number is K100874.

When did LIPOSONIX SYSTEM, MODEL 1 P00XXXX receive FDA 510(k) clearance?

LIPOSONIX SYSTEM, MODEL 1 P00XXXX received FDA 510(k) clearance on 2011-08-19, under 510(k) number K100874.

Who is the listed applicant for LIPOSONIX SYSTEM, MODEL 1 P00XXXX?

The FDA 510(k) record lists Medicis Technologies Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIPOSONIX SYSTEM, MODEL 1 P00XXXX?

The FDA product code for LIPOSONIX SYSTEM, MODEL 1 P00XXXX is OHV.

Related Clinical Trials

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Other records listing Medicis Technologies Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K112626LIPSONIX(R) SYSTEM MODEL 2

Related Devices (Code: OHV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260618Ulthera® SystemUlthera, Inc.K250418Ulthera System (UC-1 Control Unit PRIME Model 2.1)Ulthera, Inc.K243035Ulthera® SystemUlthera, Inc.K240687SofWave SystemSofwave Medical, Ltd.K233996Ulthera System (UC-1 Control Unit PRIME)Ulthera, Inc.K233104SofWave SystemSofwave Medical, Ltd.

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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