meddevicedb.com FDA Device Reference

SUMP DRAIN, W/FILTER, ARGYLE EDLICH

K770442 Class I Traditional
Decision Date
1977-03-30
Sponsor / Applicant
Sherwood Medical Industries

Technical Specification

510(k) Submission ID K770442
Product Code GBX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4200
Decision Date 1977-03-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUMP DRAIN, W/FILTER, ARGYLE EDLICH received FDA 510(k) clearance under submission number K770442, sponsored by Sherwood Medical Industries. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1977-03-30.

Classification & Regulation

This clearance is catalogued under FDA product code GBX and 21 CFR 878.4200, within the General, Plastic Surgery review panel as a Class I device.