meddevicedb.com FDA Device Reference

MEDICINE CUP

K791345 Class I Traditional
Decision Date
1979-08-03
Sponsor / Applicant
General Clinical Plastics Corp.

Technical Specification

510(k) Submission ID K791345
Product Code KYW
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6430
Decision Date 1979-08-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDICINE CUP received FDA 510(k) clearance under submission number K791345, sponsored by General Clinical Plastics 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 1979-08-03.

Classification & Regulation

This clearance is catalogued under FDA product code KYW and 21 CFR 880.6430, within the General Hospital review panel as a Class I device.