meddevicedb.com FDA Device Reference

SPONGE, RICHARDS WOUND DRAINAGE SYSTEM

K760257 Class I Traditional
Decision Date
1976-08-09
Sponsor / Applicant
Richard'S Medical Equip., Inc.

Technical Specification

510(k) Submission ID K760257
Product Code GCY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4680
Decision Date 1976-08-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPONGE, RICHARDS WOUND DRAINAGE SYSTEM received FDA 510(k) clearance under submission number K760257, sponsored by Richard'S Medical Equip., Inc.. 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 1976-08-09.

Classification & Regulation

This clearance is catalogued under FDA product code GCY and 21 CFR 878.4680, within the General, Plastic Surgery review panel as a Class I device.