meddevicedb.com FDA Device Reference

PREP TRAY, PREOPERATIVE SKIN

K781797 Class I Traditional
Decision Date
1978-11-08
Sponsor / Applicant
Pharmaseal Div., Baxter Healthcare Corp.

Technical Specification

510(k) Submission ID K781797
Product Code OJU
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1978-11-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PREP TRAY, PREOPERATIVE SKIN received FDA 510(k) clearance under submission number K781797, sponsored by Pharmaseal Div., Baxter Healthcare 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 1978-11-08.

Classification & Regulation

This clearance is catalogued under FDA product code OJU and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.