meddevicedb.com FDA Device Reference

LOW DEAD SPACE INSULIN SYRINGE

K790409 Class II Traditional
Decision Date
1979-04-24
Sponsor / Applicant
Pharmaseal Div., Baxter Healthcare Corp.

Technical Specification

510(k) Submission ID K790409
Product Code FMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 1979-04-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LOW DEAD SPACE INSULIN SYRINGE received FDA 510(k) clearance under submission number K790409, sponsored by Pharmaseal Div., Baxter Healthcare 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 1979-04-24.

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.