meddevicedb.com FDA Device Reference

BASIN, LARGE OR SMALL

K760492 Class I Traditional
Decision Date
1976-11-12
Sponsor / Applicant
Landmark Plastics

Technical Specification

510(k) Submission ID K760492
Product Code FNY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6730
Decision Date 1976-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BASIN, LARGE OR SMALL received FDA 510(k) clearance under submission number K760492, 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 FNY and 21 CFR 880.6730, within the General Hospital review panel as a Class I device.