meddevicedb.com FDA Device Reference

DISPOSABLE SURGICAL TOWEL (NON-STERILE)

K905005 Class II Traditional
Decision Date
1990-12-11
Sponsor / Applicant
Marand Products, Inc.

Technical Specification

510(k) Submission ID K905005
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1990-12-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE SURGICAL TOWEL (NON-STERILE) received FDA 510(k) clearance under submission number K905005, sponsored by Marand Products, 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 1990-12-11.

Classification & Regulation

This clearance is catalogued under FDA product code KKX and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.