FDA 510(k) Applications Submitted by RUDOLF RIESTER GMBH & CO. KG

FDA 510(k) Number Submission Date Device Name Applicant
K972301 06/19/1997 BIG BEN SQUARE, BIG BEN ROUND RUDOLF RIESTER GMBH & CO. KG
K972377 06/26/1997 RI-MEGA RUDOLF RIESTER GMBH & CO. KG
K972378 06/26/1997 SANAPHON N RUDOLF RIESTER GMBH & CO. KG
K972379 06/26/1997 PRECISA N RUDOLF RIESTER GMBH & CO. KG
K002954 09/22/2000 RI-SAN/RI-SANA BLOOD PRESSURE MANOMETERS RUDOLF RIESTER GMBH & CO. KG
K002955 09/22/2000 EMPIRE N BLOOD PRESSURE MANOMETERS RUDOLF RIESTER GMBH & CO. KG
K964338 10/31/1996 RI-TINISCOPE-SLIT/RI-TINISCOPE SPOT/RI-VISION-SLIT/RI-VISION-SPOT RUDOLF RIESTER GMBH & CO. KG


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