FDA 510(k)

VITRUVIAN INFILTRATION PUMP

K-Number: K170629 · 2017-06-22

Decision Date2017-06-22

Product CodeQPB

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VITRUVIAN INFILTRATION PUMP is a medical device manufactured by Black & Black Surgical, Inc.. It received FDA 510(k) clearance on 2017-06-22 under approval number K170629. 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 INFILTRATION PUMP?

VITRUVIAN INFILTRATION PUMP is a medical device that received FDA 510(k) clearance on 2017-06-22. It is manufactured by Black & Black Surgical, Inc.. The 510(k) number is K170629.

When was VITRUVIAN INFILTRATION PUMP approved by the FDA?

VITRUVIAN INFILTRATION PUMP received FDA 510(k) clearance on 2017-06-22, under approval number K170629.

What company makes VITRUVIAN INFILTRATION PUMP?

VITRUVIAN INFILTRATION PUMP is manufactured by Black & Black Surgical, Inc..

What is the FDA product code for VITRUVIAN INFILTRATION PUMP?

The FDA product code for VITRUVIAN INFILTRATION PUMP is QPB.

Other Devices by Black & Black Surgical, Inc.

K161722VITRUVIAN ULTIMATE ASPIRATOR K240188Vitruvian Liposaber

Related Devices (Code: QPB)

K161722VITRUVIAN ULTIMATE ASPIRATORBlack & Black Surgical, Inc. K171286PAL Multi-Use Cannulas and PAL Manual WandMicroaire Surgical Instruments, LLC K170329Basic, Dominant FlexModela AG K190551VASERlipo SystemSolta Medical 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.