Medical Device Manufacturer · DE , D-72417 Jungingen

Rudolf Riester GmbH & Co. KG - FDA 510(k) Cleared Devices

30 submissions · 26 cleared · Since 1993
30
Total
26
Cleared
0
Denied
FDA 510(k) Regulatory Record - Rudolf Riester GmbH & Co. KG Ear, Nose, Throat ✕
9 devices
1-9 of 9
Cleared May 12, 1995
PERFECT, ENT SET, PRAKTIKANT, DE LUXE
K950913 · ERA
Ear, Nose, Throat · 78d
Cleared Mar 08, 1995
H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CG
K946043 · ERA
Ear, Nose, Throat · 86d
Cleared Oct 08, 1993
STANDARD
K925752 · ERA
Ear, Nose, Throat · 329d
Cleared Oct 08, 1993
UNI III
K925753 · ERA
Ear, Nose, Throat · 329d
Cleared Oct 08, 1993
RI-MINI
K932503 · ERA
Ear, Nose, Throat · 140d
Cleared Oct 08, 1993
RI-STAR
K932505 · ERA
Ear, Nose, Throat · 140d
Cleared Oct 08, 1993
RI-SCOPE (S)
K932506 · ERA
Ear, Nose, Throat · 140d
Cleared Aug 03, 1993
OTOSCOPE
K925758 · ERA
Ear, Nose, Throat · 263d
Cleared Jul 26, 1993
UNI I
K925759 · ERA
Ear, Nose, Throat · 255d
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All30 Cardiovascular 10 Ear, Nose, Throat 9 Ophthalmic 8 Anesthesiology 1 General & Plastic Surgery 1 General Hospital 1