meddevicedb.com FDA Device Reference

FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTER

K860605 Class II Traditional
Decision Date
1986-03-24
Sponsor / Applicant
Migada, Ltd.

Technical Specification

510(k) Submission ID K860605
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1986-03-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTER received FDA 510(k) clearance under submission number K860605, sponsored by Migada, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1986-03-24.

Classification & Regulation

This clearance is catalogued under FDA product code FPA and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.