Atlas FDA

INTRA-ORAL ARTIFICIAL LARYNX

FDA 510(k) clearance K831127 · decided 1983-07-28

Clearance details

K-number
K831127
Device name
INTRA-ORAL ARTIFICIAL LARYNX
Applicant
Xomed, Inc.
Decision
Substantially Equivalent
Date received
1983-04-06
Decision date
1983-07-28
Days to decision
113 days
Clearance type
Traditional
Product code
ESE
Device class
1
Regulation number
874.3375
Medical specialty
Ear, Nose, Throat
Advisory committee
Ear, Nose, Throat
Location
Arnold, MO, 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
NU-VOIS BATTERY POWERED ARTIFICIAL LARYNX (K934483)Mountain Precision Mfg. Ltd. Co.1994-03-16
DENRICK SPEECH AID (DR-1) (K931371)Denrick Corp.1993-08-25
LECTRO-LARYNX (K923648)Bruce Medical Supply1993-04-07
AMERICAN ARTIFICIAL LARYNX (K914816)Ultravoice, Ltd.1993-02-12
ADDVOX BONE CONDUCTOR AMPLIFIER SPEAKER SYSTEM (K901503)Stanton Magnetics, Inc.1990-06-28
VOX COMPANION (K860992)Bloomfield Research and Development, Inc.1986-05-02
P.O. VOX (K860993)Bloomfield Research and Development, Inc.1986-04-25
RESNICK EMITTER, ARTIFICIAL LARYNX (K854158)Dynamed Audio, Inc.1985-12-13
ELECTRO-PALATE (K840892)Cisko Systems1984-05-22
BEAR VENTI--VOICE (K834555)Bear Medical Systems, Inc.1984-01-24
VENTI-VOICE NASAL CATHETER (K834522)Respiratory Support Products, Inc.1984-01-17
SAY (K823118)Kells Medical, Inc.1983-01-07

Recalls involving this device

No recalls on record reference this clearance.