meddevicedb.com FDA Device Reference

PROTECT-AIDS AUTOPSY UNDERGLOVE

K880440 Class I Traditional
Decision Date
1988-10-11
Sponsor / Applicant
Medical Armor Corp.

Technical Specification

510(k) Submission ID K880440
Product Code LYU
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1988-10-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROTECT-AIDS AUTOPSY UNDERGLOVE received FDA 510(k) clearance under submission number K880440, sponsored by Medical Armor 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 1988-10-11.

Classification & Regulation

This clearance is catalogued under FDA product code LYU and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class I device.