Unitron Industries, Inc. - FDA 510(k) Cleared Devices
69
Total
69
Cleared
0
Denied
FDA 510(k) Regulatory Record - Unitron Industries, Inc. Ear, Nose, Throat ✕
69 devices
Cleared
Dec 12, 1997
UNITRON MODEL F/X PROGRAMMABLE (MINI BTE)
Ear, Nose, Throat
24d
Cleared
Dec 12, 1997
UNITRON MODEL SOUND F/XD PROGRAMMABLE
Ear, Nose, Throat
24d
Cleared
Dec 12, 1997
UNITRON MODEL SOUND F/XP PROGRAMMABLE MINI BTE
Ear, Nose, Throat
24d
Cleared
May 08, 1997
UNITRON MODEL SOUND F/X CIC
Ear, Nose, Throat
72d
Cleared
Apr 24, 1997
UNITRON MODEL SOUND F/X PROGRAMMABLE ITE (SF/X PROGRAMMABLE)
Ear, Nose, Throat
72d
Cleared
Nov 27, 1996
UNITRON MODEL SOUND F/XP +4
Ear, Nose, Throat
19d
Cleared
Nov 27, 1996
UNITRON MODEL SOUND F/X +4
Ear, Nose, Throat
19d
Cleared
Nov 27, 1996
UNITRON MODEL ICON AOHPL +4
Ear, Nose, Throat
19d
Cleared
Nov 27, 1996
UNITRON MODEL ICON AOHP +4 (ICON AOHP +4)
Ear, Nose, Throat
19d
Cleared
Nov 27, 1996
UNITRON MODEL ICON AOHPD +4 (ICON AOHPD +4)
Ear, Nose, Throat
19d
Cleared
Nov 27, 1996
UNITRON MODEL SOUND F/XD +4 (SOUND F/XD +4)
Ear, Nose, Throat
19d
Cleared
Sep 06, 1996
UNITRON MODEL ICON KR
Ear, Nose, Throat
25d
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