Atlas FDA

FACEPLATE, CUSTOM IN-THE-EAR HEARING AID, FPR

FDA 510(k) clearance K862769 · decided 1986-08-13

Clearance details

K-number
K862769
Device name
FACEPLATE, CUSTOM IN-THE-EAR HEARING AID, FPR
Applicant
Maico Hearing Instruments, Inc.
Decision
Substantially Equivalent
Date received
1986-07-22
Decision date
1986-08-13
Days to decision
22 days
Clearance type
Traditional
Product code
LRB
Device class
1
Regulation number
874.3300
Medical specialty
Ear, Nose, Throat
Advisory committee
Ear, Nose, Throat
Location
Minneapolis, MN, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Maico Hearing Instruments

The Builder collects up to 8 candidate devices side by side with yours, then exports the substantial-equivalence comparison scaffold. How it works

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
FACEPLATE ASSEMBLY (K974219)Finetone Hearing Instruments1998-02-20
INTRASTAR PRE-WIRED FACEPLATE FOR IN-THE-EAR HEARING AIDS (K961593)Segi Hearing Aid Co.1996-11-07
MODULE PROGRAM (K942722)Electone, Inc.1994-09-06
AUDINA PREWIRES (FACEPLATE HEARING AID SERIES) (K942236)Audina Hearing Instrument1994-06-17
ARTISAN PROGRAMMER & HEARING AID (K935048)Telex Communications, Inc.1994-02-09
GOLD AF MODULE, ITE (K933038)Electone, Inc.1993-08-02
GOLD CD MODULE, ITE (K933040)Electone, Inc.1993-08-02
SILVER RECHARGEABLE MODULE, ITE (K933045)Electone, Inc.1993-08-02
SILVER L MODULE, ITE (K933046)Electone, Inc.1993-08-02
SILVER PPP MODULE, ITE (K933043)Electone, Inc.1993-08-02
GOLD L MODULE, ITE (K933039)Electone, Inc.1993-08-02
GOLD K AMP, ITE (K933037)Electone, Inc.1993-08-02

Recalls involving this device

No recalls on record reference this clearance.