meddevicedb.com FDA Device Reference

ABS BLOWER, ABS NOZZLE, MODEL 1001

K092801 Class II Traditional
Decision Date
2011-05-20
Sponsor / Applicant
Nimbic Systems, LLC

Technical Specification

510(k) Submission ID K092801
Product Code ORC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5070
Decision Date 2011-05-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ABS BLOWER, ABS NOZZLE, MODEL 1001 received FDA 510(k) clearance under submission number K092801, sponsored by Nimbic Systems, 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 2011-05-20.

Classification & Regulation

This clearance is catalogued under FDA product code ORC and 21 CFR 878.5070, within the General, Plastic Surgery review panel as a Class II device.