meddevicedb.com FDA Device Reference

MEDARMOR FINGER TIP, PUNCTURE RESISTANT UNDERGLOVE

K923229 Class I Traditional
Decision Date
1993-05-07
Sponsor / Applicant
Medical Armor Corp.

Technical Specification

510(k) Submission ID K923229
Product Code LYU
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1993-05-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDARMOR FINGER TIP, PUNCTURE RESISTANT UNDERGLOVE received FDA 510(k) clearance under submission number K923229, 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 1993-05-07.

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.