Philips Int'L B.V.

Philips Int'L B.V. holds 11 FDA 510(k) medical device clearances, first cleared 1985, most recent 1992.

Top product codes for Philips Int'L B.V.

FTC — General, Plastic Surgery9 devices
ESD — Ear, Nose, Throat2 devices

Recent clearances by Philips Int'L B.V.

K920134 — PHILIPS 41 SERIES RAINBOWCode ESD·1992-01-24
K920142 — PHILIPS M60 SERIESCode ESD·1992-01-23
K852348 — PHILIPS SOLARIUM HP 3134Code FTC·1985-06-27
K851533 — PHILIPS UV-A SDARIUM TYPE HP 3148(CFR 21 SUNLAMPCode FTC·1985-05-01
K851534 — PHILIPS UV-A SOLARIUM TYPE HP 3150Code FTC·1985-05-01
K851535 — PHILIPS UV-A SOLARIUM TYPE HP 3140Code FTC·1985-05-01
K851536 — PHILIPS UV-A SOLARIUM TYPE HP 3141Code FTC·1985-05-01
K850203 — PHILIPS UV-A SOLARIUM TYPE HP 3016-SUNLAMPCode FTC·1985-02-21
K850204 — PHILIPS UV-A SOLARIUM TYPE HP 3130-SUNLAMPCode FTC·1985-02-21
K850205 — PHILIPS UV-A SOLARIUM TYPE HP 3127-SUNLAMPCode FTC·1985-02-21
K850206 — PHILIPS UV-A SOLARIUM TYPE HP 3126-SUNLAMPCode FTC·1985-02-21

Data sourced from openFDA. This site is unofficial and independent of the FDA.