meddevicedb.com FDA Device Reference

SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN

K926496 Class I Traditional
Decision Date
1995-05-24
Sponsor / Applicant
Sil-Med Corp.

Technical Specification

510(k) Submission ID K926496
Product Code GBX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4200
Decision Date 1995-05-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN received FDA 510(k) clearance under submission number K926496, sponsored by Sil-Med Corp.. 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 1995-05-24.

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.