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PARENTERAL INFUSION CONTROLLER, ELEC.

K780106 Class II Traditional
Decision Date
1978-02-21
Sponsor / Applicant
National Patent Development Corp.

Technical Specification

510(k) Submission ID K780106
Product Code FLN
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2420
Decision Date 1978-02-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PARENTERAL INFUSION CONTROLLER, ELEC. received FDA 510(k) clearance under submission number K780106, 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 1978-02-21.

Classification & Regulation

This clearance is catalogued under FDA product code FLN and 21 CFR 880.2420, within the General Hospital review panel as a Class II device.