meddevicedb.com FDA Device Reference

PAL Infiltration System

K220318 Class II Traditional
Decision Date
2022-10-14
Sponsor / Applicant
Microaire Surgical Instruments, LLC

Technical Specification

510(k) Submission ID K220318
Product Code QPB
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5040
Decision Date 2022-10-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PAL Infiltration System received FDA 510(k) clearance under submission number K220318, sponsored by Microaire Surgical Instruments, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2022-10-14.

Classification & Regulation

This clearance is catalogued under FDA product code QPB and 21 CFR 878.5040, within the General, Plastic Surgery review panel as a Class II device.