meddevicedb.com FDA Device Reference

CLEAR PLASTIC CONNECTING TUBES

K800879 Class II Traditional
Decision Date
1980-06-17
Sponsor / Applicant
Harvard Laboratories

Technical Specification

510(k) Submission ID K800879
Product Code FPK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1980-06-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLEAR PLASTIC CONNECTING TUBES received FDA 510(k) clearance under submission number K800879, sponsored by Harvard Laboratories. 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 1980-06-17.

Classification & Regulation

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