Medical Device Manufacturer · DE , D-72417 Jungingen

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

30 submissions · 26 cleared · Since 1993

Total

Cleared

Denied

Rudolf Riester GmbH & Co. KG has 26 FDA 510(k) cleared medical devices. Based in D-72417 Jungingen, DE.

Historical record: 26 cleared submissions from 1993 to 2000.

Browse the FDA 510(k) cleared devices submitted by Rudolf Riester GmbH & Co. KG Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Rudolf Riester GmbH & Co. KG

30 devices

1-12 of 30

Cleared Dec 21, 2000

RI-SAN/RI-SANA BLOOD PRESSURE MANOMETERS

K002954 · DXQ

Cardiovascular · 90d

Cleared Dec 21, 2000

EMPIRE N BLOOD PRESSURE MANOMETERS

BIG BEN SQUARE, BIG BEN ROUND

K972301 · DXQ

Cardiovascular · 90d

Cleared Jan 09, 1997

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

K964338 · HKM

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...

K950914 · HLJ

Ophthalmic · 151d

Cleared May 12, 1995

PERFECT, ENT SET, PRAKTIKANT, DE LUXE

K950913 · ERA

Ear, Nose, Throat · 78d

Cleared May 08, 1995

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

K945541 · HKY

Ophthalmic · 179d

Cleared Mar 20, 1995

MCINTOSH, MILLER, FOREGGER BABY

K945425 · CCW

Anesthesiology · 136d

Cleared Mar 08, 1995

H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CG

K946043 · ERA

Ear, Nose, Throat · 86d

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

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