meddevicedb.com FDA Device Reference

PAL Single-Use Cannulas

K192694 Class II Traditional
Decision Date
2020-05-14
Sponsor / Applicant
Microaire Surgical Instruments

Technical Specification

510(k) Submission ID K192694
Product Code QPB
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5040
Decision Date 2020-05-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PAL Single-Use Cannulas received FDA 510(k) clearance under submission number K192694, sponsored by Microaire Surgical Instruments. 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 2020-05-14.

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.