meddevicedb.com FDA Device Reference

HEMO-NATE SYRINGE BLOOD FILTER

K781815 Class II Traditional
Decision Date
1979-02-27
Sponsor / Applicant
Gisco Intl.

Technical Specification

510(k) Submission ID K781815
Product Code FPB
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1979-02-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMO-NATE SYRINGE BLOOD FILTER received FDA 510(k) clearance under submission number K781815, sponsored by Gisco Intl.. 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 1979-02-27.

Classification & Regulation

This clearance is catalogued under FDA product code FPB and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.