meddevicedb.com FDA Device Reference

STERILE AIR SYRINGE

K780550 Class II Traditional
Decision Date
1978-04-19
Sponsor / Applicant
National Patent Development Corp.

Technical Specification

510(k) Submission ID K780550
Product Code FMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 1978-04-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILE AIR SYRINGE received FDA 510(k) clearance under submission number K780550, sponsored by National Patent Development Corp.. 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 1978-04-19.

Classification & Regulation

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