FDA 510(k)

VASERlipo System

K-Number: K190551 · 2019-05-01

Decision Date2019-05-01

Product CodeQPB

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VASERlipo System is a medical device manufactured by Solta Medical. It received FDA 510(k) clearance on 2019-05-01 under approval number K190551. The device is classified under product code QPB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASERlipo System?

VASERlipo System is a medical device that received FDA 510(k) clearance on 2019-05-01. It is manufactured by Solta Medical. The 510(k) number is K190551.

When was VASERlipo System approved by the FDA?

VASERlipo System received FDA 510(k) clearance on 2019-05-01, under approval number K190551.

What company makes VASERlipo System?

VASERlipo System is manufactured by Solta Medical.

What is the FDA product code for VASERlipo System?

The FDA product code for VASERlipo System is QPB.

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Other Devices by Solta Medical

K170758Thermage FLX System and Accessories K173759Thermage CPT System and Accessories K190555PowerX Lipo System K242142Fraxel® FTX Laser System

Related Devices (Code: QPB)

K161722VITRUVIAN ULTIMATE ASPIRATORBlack & Black Surgical, Inc. K171286PAL Multi-Use Cannulas and PAL Manual WandMicroaire Surgical Instruments, LLC K170629VITRUVIAN INFILTRATION PUMPBlack & Black Surgical, Inc. K170329Basic, Dominant FlexModela AG K190555PowerX Lipo SystemSolta Medical K192694PAL Single-Use CannulasMicroaire Surgical Instruments

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.