Medical Device Manufacturer · US , Mahwah , NJ

Philips Hearing Instruments Co. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1991

Recent clearances: D72 DIGITAL, PHILIPS S1694, S1695, M11 SERIES: M11, M11M

Total

Cleared

Denied

Philips Hearing Instruments Co. has 20 FDA 510(k) cleared ear, nose, throat devices. Based in Mahwah, US.

Historical record: 20 cleared submissions from 1991 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.

Philips Hearing Instruments Co. is one of 15035 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Philips Hearing Instruments Co.

20 devices

1-12 of 20

Cleared Oct 17, 1997

D72 DIGITAL

K972818 · ESD

Ear, Nose, Throat · 80d

Cleared Jun 06, 1997

PHILIPS S1694, S1695

K971804 · ESD

Ear, Nose, Throat · 23d

Cleared Jan 24, 1997

M11 SERIES: M11, M11M

K965088 · ESD

Ear, Nose, Throat · 36d

Cleared Aug 02, 1996

PHILIPS 71 SERIES

K961770 · ESD

Ear, Nose, Throat · 86d

Cleared Jul 28, 1995

HEARING AID

K952658 · ESD

Ear, Nose, Throat · 46d

Cleared Dec 27, 1994

MO4 SERIES

K944404 · ESD

Ear, Nose, Throat · 110d

Cleared Aug 18, 1994

MO6 SERIES

K943670 · ESD

Ear, Nose, Throat · 23d

Cleared Aug 09, 1994

PHILIPS M38 SERIES

K943395 · ESD

Ear, Nose, Throat · 26d

Cleared Jun 17, 1994

PHILIPS 61 SERIES

K942164 · ESD

Ear, Nose, Throat · 44d

Cleared Sep 07, 1993

PHILIPS 45 SERIES

K933850 · ESD

Ear, Nose, Throat · 32d

Cleared Aug 11, 1992

PHILIP XP SERIES, IN-THE CANAL HEARING AID

K921725 · ESD

Ear, Nose, Throat · 124d

Cleared May 22, 1992

PHILIPS 31 SERIES IN THE EAR HEARING AID

K921463 · ESD

Ear, Nose, Throat · 56d

Philips Hearing Instruments Co. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Philips Hearing Instruments Co.

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