meddevicedb.com FDA Device Reference

ASEPTEX 1809 FLUID-RESISTANT MOLDED SURGICAL MASK

K881618 Class II Traditional
Decision Date
1988-05-09
Sponsor / Applicant
3M Company

Technical Specification

510(k) Submission ID K881618
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1988-05-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ASEPTEX 1809 FLUID-RESISTANT MOLDED SURGICAL MASK received FDA 510(k) clearance under submission number K881618, sponsored by 3M Company. 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 1988-05-09.

Classification & Regulation

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