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 Ophthalmic ✕

8 devices

1-8 of 8

Cleared Jan 09, 1997

RI-TINISCOPE-SLIT/RI-TINISCOPE SPOT/RI-VISION-SLIT/RI-VISION-SPOT

Ophthalmic · 70d

Cleared Jul 24, 1995

RI-FORMER WALL MODEL 2,5 V/220 V OR 110 V 3,5 V/220 V OR 110 V, RI-FORMER...

Ophthalmic · 151d

Cleared May 08, 1995

SCHIOTZ TONOMETER SPEC. 5 STRAIGHT, INCLINED, 3INCLINED SCALE

Ophthalmic · 179d

Cleared Jan 17, 1995

RI-SCOPE S OTOSCOPE

Ophthalmic · 62d

Cleared Dec 03, 1993

Ophthalmic · 385d

Cleared Oct 18, 1993

Ophthalmic · 339d

Cleared Oct 15, 1993

Ophthalmic · 147d

Cleared Aug 03, 1993

Ophthalmic · 263d