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FDA 510(k)

Vitruvian Liposaber

K-Number: K240188 · 2024-09-13

ApplicantBlack & Black Surgical, Inc.
Decision Date2024-09-13
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Vitruvian Liposaber is a medical device manufactured by Black & Black Surgical, Inc.. It received FDA 510(k) clearance on 2024-09-13 under approval number K240188. 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 Vitruvian Liposaber?

Vitruvian Liposaber is a medical device that received FDA 510(k) clearance on 2024-09-13. It is manufactured by Black & Black Surgical, Inc.. The 510(k) number is K240188.

When was Vitruvian Liposaber approved by the FDA?

Vitruvian Liposaber received FDA 510(k) clearance on 2024-09-13, under approval number K240188.

What company makes Vitruvian Liposaber?

Vitruvian Liposaber is manufactured by Black & Black Surgical, Inc..

What is the FDA product code for Vitruvian Liposaber?

The FDA product code for Vitruvian Liposaber is QPB.

Other Devices by Black & Black Surgical, Inc.

K161722VITRUVIAN ULTIMATE ASPIRATOR K170629VITRUVIAN INFILTRATION PUMP

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 K190551VASERlipo SystemSolta Medical K190555PowerX Lipo SystemSolta Medical

Official Source

View on FDA Database →

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

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