Medical Device Manufacturer · US , Mchenry , IL

Electone, Inc. - FDA 510(k) Cleared Devices

73 submissions · 73 cleared · Since 1981

Total

Cleared

Denied

Electone, Inc. has 73 FDA 510(k) cleared ear, nose, throat devices. Based in Mchenry, US.

Historical record: 73 cleared submissions from 1981 to 1997.

Browse the complete list of FDA 510(k) cleared ear, nose, throat devices from this manufacturer. Filter by specialty or product code using the sidebar.

Electone, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Electone, Inc.

73 devices

1-12 of 73

Cleared Sep 23, 1997

Z DEQ-II

K973266 · ESD

Ear, Nose, Throat · 25d

Cleared Apr 18, 1996

AM 400

K961084 · ESD

Ear, Nose, Throat · 30d

Cleared Feb 22, 1996

SONATA U-01

K955702 · ESD

Ear, Nose, Throat · 69d

Cleared Aug 22, 1995

Z20

K953047 · ESD

Ear, Nose, Throat · 53d

Cleared Aug 22, 1995

Z33

K953050 · ESD

Ear, Nose, Throat · 53d

Cleared Aug 15, 1995

Z22

K953048 · ESD

Ear, Nose, Throat · 46d

Cleared Aug 15, 1995

Z24

K953049 · ESD

Ear, Nose, Throat · 46d

Cleared Aug 15, 1995

Z35

K953051 · ESD

Ear, Nose, Throat · 46d

Cleared Aug 15, 1995

AM 260 K-AMP

K953052 · ESD

Ear, Nose, Throat · 46d

Cleared Aug 15, 1995

AM 260 PP

K953053 · ESD

Ear, Nose, Throat · 46d

Cleared Aug 15, 1995

AM 260 OHM

K953054 · ESD

Ear, Nose, Throat · 46d

Cleared Jul 11, 1995

GOLD CD ULTRA MINI CANAL - MODULE

K951642 · ESD

Ear, Nose, Throat · 92d

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Electone, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Electone, Inc.

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