Atlas FDA

FACEPLATE ASSEMBLY

FDA 510(k) clearance K974219 · decided 1998-02-20

Clearance details

K-number
K974219
Device name
FACEPLATE ASSEMBLY
Applicant
Finetone Hearing Instruments
Decision
Substantially Equivalent
Date received
1997-11-10
Decision date
1998-02-20
Days to decision
102 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
Scarborough, ME, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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

RecordFirmDate
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
SILVER LD MODULE, ITE (K933044)Electone, Inc.1993-08-02

Recalls involving this device

No recalls on record reference this clearance.