meddevicedb.com FDA Device Reference

FLU-ADMIN, MODELS 60150, 60150C, 60151C, 60153C, 60160

K082027 Class II Traditional
Decision Date
2009-02-13
Sponsor / Applicant
Genesis Bps, LLC

Technical Specification

510(k) Submission ID K082027
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 2009-02-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLU-ADMIN, MODELS 60150, 60150C, 60151C, 60153C, 60160 received FDA 510(k) clearance under submission number K082027, sponsored by Genesis Bps, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2009-02-13.

Classification & Regulation

This clearance is catalogued under FDA product code FPA and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.