FDA 510(k) Applications Submitted by DON CAMPBELL
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K973972 |
10/20/1997 |
PERFECT EAR/ MINI-CANAL/ PE-M, PE-ML, PE-MD), PERFECT EAR/ C.I.C./ (PEC, PE-CD) (WITH OR WITHOUT RID-WAX BARRIER) |
PERFECT EAR |
| K093715 |
12/01/2009 |
EVOK 900 SERIES HEARING AID/TINNITUS MASKER OPTION DEVICE |
MAGNATONE HEARING AID CORP. DBA PERSONA MEDICAL |
| K973665 |
09/25/1997 |
MAGNATONE / STERLING/ ST; MAGNATONE/DB; MAGNATONE/ LIBERTY/ LB; MAGNATONE/ PEARL/PH C.I.C., S.P.I., ONE TOUCH, DESIGNER |
MAGNATONE HEARING AID CORP. |
| K973861 |
10/09/1997 |
FUTURA 67M, 68M, MEGAPOWERMP97, INTEGRA 70,71,72,73, SUPRA 51,52, SUPRA 56,57,58,59, SUPREMA 45, 46, 47,48 |
MAGNATONE HEARING AID CORP. |
| K960410 |
01/29/1996 |
PERFECT EAR PE/PE-AGC/PE-B/PE-PWR |
PERFECT EAR |
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