meddevicedb.com FDA Device Reference

CUP, DISPOSABLE MEDICINE

K760517 Class I Traditional
Decision Date
1976-11-12
Sponsor / Applicant
Landmark Plastics

Technical Specification

510(k) Submission ID K760517
Product Code KYX
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6430
Decision Date 1976-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CUP, DISPOSABLE MEDICINE received FDA 510(k) clearance under submission number K760517, sponsored by Landmark Plastics. 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 1976-11-12.

Classification & Regulation

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