meddevicedb.com FDA Device Reference

MICRO Z BLOOD COLLECTING NEEDLES

K823696 Class II Traditional
Decision Date
1983-01-26
Sponsor / Applicant
Hospital Products Co.

Technical Specification

510(k) Submission ID K823696
Product Code FMI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 1983-01-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICRO Z BLOOD COLLECTING NEEDLES received FDA 510(k) clearance under submission number K823696, sponsored by Hospital Products Co.. 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 1983-01-26.

Classification & Regulation

This clearance is catalogued under FDA product code FMI and 21 CFR 880.5570, within the General Hospital review panel as a Class II device.