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PHD-36 PHYSIOLOGICAL SIGNAL AMPLIFIER

K860289 Class II Traditional
Decision Date
1986-08-25
Sponsor / Applicant
Professional Health Technologies, Inc.

Technical Specification

510(k) Submission ID K860289
Product Code GWL
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1835
Decision Date 1986-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHD-36 PHYSIOLOGICAL SIGNAL AMPLIFIER received FDA 510(k) clearance under submission number K860289, sponsored by Professional Health Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1986-08-25.

Classification & Regulation

This clearance is catalogued under FDA product code GWL and 21 CFR 882.1835, within the Neurology review panel as a Class II device.