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Heartland Health Surgical Mask

K212366 Class II Abbreviated
Decision Date
2022-02-19
Sponsor / Applicant
Heartland Health Products

Technical Specification

510(k) Submission ID K212366
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2022-02-19
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Heartland Health Surgical Mask received FDA 510(k) clearance under submission number K212366, sponsored by Heartland Health Products. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2022-02-19.

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.