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TENCEL X-RAY DETECTABLE SPONGES/LAP PADS

K932846 Class I Traditional
Decision Date
1993-12-09
Sponsor / Applicant
Courtaulds Fibers, Inc.

Technical Specification

510(k) Submission ID K932846
Product Code GDY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4450
Decision Date 1993-12-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TENCEL X-RAY DETECTABLE SPONGES/LAP PADS received FDA 510(k) clearance under submission number K932846, sponsored by Courtaulds Fibers, 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 1993-12-09.

Classification & Regulation

This clearance is catalogued under FDA product code GDY and 21 CFR 878.4450, within the General, Plastic Surgery review panel as a Class I device.