FACEPLATE, CUSTOM IN-THE-EAR HEARING AID, FPR— 510(k) K862769

Name: FDA 510(k) clearance K862769
Creator: U.S. Food and Drug Administration
Published: 1986-08-13

Substantially Equivalent

Maico Hearing Instruments, Inc.

FDA 510(k) clearance K862769 for FACEPLATE, CUSTOM IN-THE-EAR HEARING AID, FPR, Substantially Equivalent on 1986-08-13. Applicant: Maico Hearing Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Maico Hearing Instruments, Inc.
Product code: Code LRB
Device class: Class 1
Regulation: 21 CFR 874.3300
Advisory panel: Ear, Nose, Throat
Date received: 1986-07-22
Decision date: 1986-08-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LRB

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K974219 — FACEPLATE ASSEMBLY1998-02-20
K961593 — INTRASTAR PRE-WIRED FACEPLATE FOR IN-THE-EAR HEARING AIDS1996-11-07
K942722 — MODULE PROGRAM1994-09-06
K942236 — AUDINA PREWIRES (FACEPLATE HEARING AID SERIES)1994-06-17
K935048 — ARTISAN PROGRAMMER & HEARING AID1994-02-09

More clearances from Maico Hearing Instruments, Inc.

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K960031 — AUDIOFLEX 1201996-03-07
K954054 — MAICO PRODIGY CIC SERIES1995-09-28
K953161 — MAICO MA630D AUDIOMETER WITH OPTIONAL REFLEX DECAY & EUSTACHIAN TUBE FUNCTION1995-07-24
K950637 — MAICO IN-THE-EAR MODEL RD-312 CIC1995-03-21
K946253 — MAICO IN-THE-EAR MODEL RD 2011995-01-30

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