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FDA 510(k)

PAL Multi-Use Cannulas and PAL Manual Wand

K-Number: K171286 · 2017-10-13

ApplicantMicroaire Surgical Instruments, LLC
Decision Date2017-10-13
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PAL Multi-Use Cannulas and PAL Manual Wand is a medical device manufactured by Microaire Surgical Instruments, LLC. It received FDA 510(k) clearance on 2017-10-13 under approval number K171286. 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 PAL Multi-Use Cannulas and PAL Manual Wand?

PAL Multi-Use Cannulas and PAL Manual Wand is a medical device that received FDA 510(k) clearance on 2017-10-13. It is manufactured by Microaire Surgical Instruments, LLC. The 510(k) number is K171286.

When was PAL Multi-Use Cannulas and PAL Manual Wand approved by the FDA?

PAL Multi-Use Cannulas and PAL Manual Wand received FDA 510(k) clearance on 2017-10-13, under approval number K171286.

What company makes PAL Multi-Use Cannulas and PAL Manual Wand?

PAL Multi-Use Cannulas and PAL Manual Wand is manufactured by Microaire Surgical Instruments, LLC.

What is the FDA product code for PAL Multi-Use Cannulas and PAL Manual Wand?

The FDA product code for PAL Multi-Use Cannulas and PAL Manual Wand is QPB.

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Related Devices (Code: QPB)

K161722VITRUVIAN ULTIMATE ASPIRATORBlack & Black Surgical, Inc. K170629VITRUVIAN INFILTRATION PUMPBlack & Black Surgical, Inc. K170329Basic, Dominant FlexModela AG K190551VASERlipo SystemSolta Medical K190555PowerX Lipo SystemSolta Medical K192694PAL Single-Use CannulasMicroaire Surgical Instruments

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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