HEARING AID VARIOUS MODELS— 510(k) K821972

Name: FDA 510(k) clearance K821972
Creator: U.S. Food and Drug Administration
Published: 1982-07-20

Substantially Equivalent

Panasonic Co. Div. Matsu Elec. Corp. America

FDA 510(k) clearance K821972 for HEARING AID VARIOUS MODELS, Substantially Equivalent on 1982-07-20. Applicant: Panasonic Co. Div. Matsu Elec. Corp. America. Device class: 1.

Clearance details

Applicant: Panasonic Co. Div. Matsu Elec. Corp. America
Product code: Code ESD
Device class: Class 1
Regulation: 21 CFR 874.3300
Advisory panel: Ear, Nose, Throat
Date received: 1982-07-02
Decision date: 1982-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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 Panasonic Co. Div. Matsu Elec. Corp. America

view all

K860634 — PANASONIC BLOOD PRESSURE METER, ZH-852AP, ZH-858PP1986-07-01
K832076 — ELECTRONIC BLOOD PRESS. METER EN-2121984-10-26
K841103 — NONINVASIVE BLOOD PRESSURE MEASURE SYS1984-10-26
K833510 — PANASONIC WH-50 HEARING AID1983-11-14
K832075 — ELECTRONIC BLOOD PRESS. METER-ZH-820P1983-08-12

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