meddevicedb.com FDA Device Reference

EYE PADS CAT.#581-599

K801995 Class I Traditional
Decision Date
1980-09-09
Sponsor / Applicant
Pollak (Intl.), Ltd.

Technical Specification

510(k) Submission ID K801995
Product Code HMP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4440
Decision Date 1980-09-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EYE PADS CAT.#581-599 received FDA 510(k) clearance under submission number K801995, sponsored by Pollak (Intl.), Ltd.. 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 1980-09-09.

Classification & Regulation

This clearance is catalogued under FDA product code HMP and 21 CFR 878.4440, within the General, Plastic Surgery review panel as a Class I device.