meddevicedb.com FDA Device Reference

SPUNGUARD PLUS SURGICAL DRAPE

K862801 Class II Traditional
Decision Date
1986-08-07
Sponsor / Applicant
Kimberly-Clark Corp.

Technical Specification

510(k) Submission ID K862801
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1986-08-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPUNGUARD PLUS SURGICAL DRAPE received FDA 510(k) clearance under submission number K862801, sponsored by Kimberly-Clark 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 1986-08-07.

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.