AUDIOTECH MODEL DP— 510(k) K931975

Name: FDA 510(k) clearance K931975
Creator: U.S. Food and Drug Administration
Published: 1993-06-22

Substantially Equivalent

Muskogee Regional Hearing Aid Lab

FDA 510(k) clearance K931975 for AUDIOTECH MODEL DP, Substantially Equivalent on 1993-06-22. Applicant: Muskogee Regional Hearing Aid Lab. Device class: 1.

Clearance details

Applicant: Muskogee Regional Hearing Aid Lab
Product code: Code ESD
Device class: Class 1
Regulation: 21 CFR 874.3300
Advisory panel: Ear, Nose, Throat
Date received: 1993-04-22
Decision date: 1993-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Muskogee, OK, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code ESD

view all

K232999 — Lyric4 Hearing Aid2024-04-11
K130790 — LYRIC22013-06-27
K081136 — LYRIC HEARING AID2008-05-08
K021867 — INSOUND XT SERIES HEARING AID2002-11-19
K003558 — TCI COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION)2001-04-24

More clearances from Muskogee Regional Hearing Aid Lab

view all

Data sourced from openFDA. This site is unofficial and independent of the FDA.