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SURGICAL EYE PACK

K851906 Class I Traditional
Decision Date
1985-05-21
Sponsor / Applicant
Xanmed Corp.

Technical Specification

510(k) Submission ID K851906
Product Code HMP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4440
Decision Date 1985-05-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL EYE PACK received FDA 510(k) clearance under submission number K851906, sponsored by Xanmed 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 1985-05-21.

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.