Philips Hearing Instruments Co.
Philips Hearing Instruments Co. holds FDA 510(k) medical device clearances, first cleared 1991, most recent 1997.
Top product codes for Philips Hearing Instruments Co.
Recent clearances by Philips Hearing Instruments Co.
- K972818 — D72 DIGITAL
- K971804 — PHILIPS S1694, S1695
- K965088 — M11 SERIES: M11, M11M
- K961770 — PHILIPS 71 SERIES
- K952658 — HEARING AID
- K944404 — MO4 SERIES
- K943670 — MO6 SERIES
- K943395 — PHILIPS M38 SERIES
- K942164 — PHILIPS 61 SERIES
- K933850 — PHILIPS 45 SERIES
- K921725 — PHILIP XP SERIES, IN-THE CANAL HEARING AID
- K921463 — PHILIPS 31 SERIES IN THE EAR HEARING AID
- K915252 — PHILIPS P74P BEHIND-THE-EAR HEARING AID
- K914800 — P54 BTE HEARING AID
- K913389 — PHILIPS S1594 OTB HEARING AID
- K913390 — M32 IN-THE-EAR HEARING AID
- K912339 — PHILIPS M30 IN-THE-EAR HEARING AID
- K910743 — PHILIPS MODEL S46-OL BTE HEARING AID
- K910744 — PHILIPS MODEL S46-O BTE HEARING AID
- K910206 — PHILIPS MODEL S47 BTE HEARING AID
Data sourced from openFDA. This site is unofficial and independent of the FDA.