meddevicedb.com FDA Device Reference

1 ML FIXED NEEDLE, 3 ML LUER LOCK, 5 ML LUER LOCK, 10 ML LUER LOCK, 20 ML LUERL LOCK SAFETY SYRINGES

K092430 Class II Special
Decision Date
2009-09-04
Sponsor / Applicant
Inviro Medical Devices, Inc.

Technical Specification

510(k) Submission ID K092430
Product Code MEG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 2009-09-04
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

1 ML FIXED NEEDLE, 3 ML LUER LOCK, 5 ML LUER LOCK, 10 ML LUER LOCK, 20 ML LUERL LOCK SAFETY SYRINGES received FDA 510(k) clearance under submission number K092430, sponsored by Inviro Medical Devices, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2009-09-04.

Classification & Regulation

This clearance is catalogued under FDA product code MEG and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.