Cleared Traditional

SIEMENS MODEL 584-P-GC

K930998 · Siemens Hearing Instruments, Inc. · Ear, Nose, Throat

Apr 1993

Decision

45d

Days

Class 1

Risk

About This 510(k) Submission

K930998 is an FDA 510(k) clearance for the SIEMENS MODEL 584-P-GC, a Hearing Aid, Air-conduction, Prescription (Class I — General Controls, product code ESD), submitted by Siemens Hearing Instruments, Inc. (Piscataway, US). The FDA issued a Cleared decision on April 12, 1993, 45 days after receiving the submission on February 26, 1993. This device falls under the Ear, Nose, Throat review panel. Regulated under 21 CFR 874.3300.

Submission Details

510(k) Number	K930998 FDA.gov
FDA Decision	Cleared SESE
Date Received	February 26, 1993
Decision Date	April 12, 1993
Days to Decision	45 days
Submission Type	Traditional
Review Panel	Ear, Nose, Throat (EN)
Summary	Statement

Device Classification

Product Code	ESD — Hearing Aid, Air-conduction, Prescription
Device Class	Class I — General Controls
CFR Regulation	21 CFR 874.3300
Definition	An Air-conduction Hearing Aid Is A Wearable Sound Amplifying Device Intended To Compensate For Impaired Hearing That Conducts Sound To The Ear Through The Air. This Is A Prescription Hearing Aid.