Larynx, Artificial (Battery-Powered)
FDA product code ESE · 13 cleared devices
Class 1
Ear, Nose, Throat
- Regulation
- 21 CFR 874.3375
- Review panel
- EN
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1983-01-07 – 1994-03-16
ESE
1994-03-16
ESE
1993-08-25
DENRICK SPEECH AID (DR-1)
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ESE
1993-04-07
LECTRO-LARYNX
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ESE
1993-02-12
AMERICAN ARTIFICIAL LARYNX
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ESE
1990-06-28
ADDVOX BONE CONDUCTOR AMPLIFIER SPEAKER SYSTEM
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ESE
1986-05-02
VOX COMPANION
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ESE
1986-04-25
P.O. VOX
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ESE
1985-12-13
RESNICK EMITTER, ARTIFICIAL LARYNX
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ESE
1984-05-22
ELECTRO-PALATE
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ESE
1984-01-24
BEAR VENTI--VOICE
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ESE
1984-01-17
VENTI-VOICE NASAL CATHETER
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ESE
1983-07-28
INTRA-ORAL ARTIFICIAL LARYNX
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ESE
1983-01-07
SAY
View details →No matching devices.
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