meddevicedb.com FDA Device Reference

SQUARE ONE SAFETY SYRINGE

K955030 Class II Traditional
Decision Date
1995-12-15
Sponsor / Applicant
Square One Medical, LP

Technical Specification

510(k) Submission ID K955030
Product Code MEG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 1995-12-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SQUARE ONE SAFETY SYRINGE received FDA 510(k) clearance under submission number K955030, sponsored by Square One Medical, LP. 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 1995-12-15.

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.