meddevicedb.com FDA Device Reference

IMPEDANCE ANALYZER MODELS MD-2, MD-P

K895783 Class II Traditional
Decision Date
1989-12-05
Sponsor / Applicant
Singer Medical Products, Inc.

Technical Specification

510(k) Submission ID K895783
Product Code ETY
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.1090
Decision Date 1989-12-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMPEDANCE ANALYZER MODELS MD-2, MD-P received FDA 510(k) clearance under submission number K895783, sponsored by Singer Medical Products, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1989-12-05.

Classification & Regulation

This clearance is catalogued under FDA product code ETY and 21 CFR 874.1090, within the Ear, Nose, Throat review panel as a Class II device.