Medical Device Manufacturer · NL , The Netherlands

Philips Int'L B.V. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1985

Total

Cleared

Denied

Philips Int'L B.V. has 11 FDA 510(k) cleared general & plastic surgery devices. Based in The Netherlands, NL.

Historical record: 11 cleared submissions from 1985 to 1992.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

Philips Int'L B.V. is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Philips Int'L B.V.

11 devices

1-11 of 11

Cleared Jan 24, 1992

PHILIPS 41 SERIES RAINBOW

K920134 · ESD

Ear, Nose, Throat · 11d

Cleared Jan 23, 1992

PHILIPS M60 SERIES

K920142 · ESD

Ear, Nose, Throat · 10d

Cleared Jun 27, 1985

PHILIPS SOLARIUM HP 3134

K852348 · FTC

General & Plastic Surgery · 27d

Cleared May 01, 1985

PHILIPS UV-A SDARIUM TYPE HP 3148(CFR 21 SUNLAMP

K851533 · FTC

General & Plastic Surgery · 15d

Cleared May 01, 1985

PHILIPS UV-A SOLARIUM TYPE HP 3150

K851534 · FTC

General & Plastic Surgery · 15d

Cleared May 01, 1985

PHILIPS UV-A SOLARIUM TYPE HP 3140

K851535 · FTC

General & Plastic Surgery · 15d

Cleared May 01, 1985

PHILIPS UV-A SOLARIUM TYPE HP 3141

K851536 · FTC

General & Plastic Surgery · 15d

Cleared Feb 21, 1985

PHILIPS UV-A SOLARIUM TYPE HP 3016-SUNLAMP

K850203 · FTC

General & Plastic Surgery · 34d

Cleared Feb 21, 1985

PHILIPS UV-A SOLARIUM TYPE HP 3130-SUNLAMP

K850204 · FTC

General & Plastic Surgery · 34d

Cleared Feb 21, 1985

PHILIPS UV-A SOLARIUM TYPE HP 3127-SUNLAMP

K850205 · FTC

General & Plastic Surgery · 34d

Cleared Feb 21, 1985

PHILIPS UV-A SOLARIUM TYPE HP 3126-SUNLAMP

K850206 · FTC

General & Plastic Surgery · 34d

Philips Int'L B.V. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Philips Int'L B.V.

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