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Rudolf Riester GmbH & Co. KG

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
30
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K002954RI-SAN/RI-SANA BLOOD PRESSURE MANOMETERSDecember 21, 2000
K002955EMPIRE N BLOOD PRESSURE MANOMETERSDecember 21, 2000
K972377RI-MEGASeptember 24, 1997
K972378SANAPHON NSeptember 24, 1997
K972379PRECISA NSeptember 24, 1997
K972301BIG BEN SQUARE, BIG BEN ROUNDSeptember 17, 1997
K964338RI-TINISCOPE-SLIT/RI-TINISCOPE SPOT/RI-VISION-SLIT/RI-VISION-SPOTJanuary 9, 1997
K950914RI-FORMER WALL MODEL 2,5 V/220 V OR 110 V 3,5 V/220 V OR 110 V, RI-FORMER ANAESTHETIC MODEL 2,5 V/22July 24, 1995
K950913PERFECT, ENT SET, PRAKTIKANT, DE LUXEMay 12, 1995
K945541SCHIOTZ TONOMETER SPEC. 5 STRAIGHT, INCLINED, 3INCLINED SCALEMay 8, 1995
K945425MCINTOSH, MILLER, FOREGGER BABYMarch 20, 1995
K946043H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CGMarch 8, 1995
K945640RI-SCOPE S OTOSCOPEJanuary 17, 1995
K945507H 5100, H 5200, H 5300December 9, 1994
K942777MINIMUS II; MINIMUS II COLOR; BABYPHONJuly 27, 1994
K925295EXACTA-SPEZIALMarch 25, 1994
K925294PRECISAFebruary 23, 1994
K925297RI-MEDJanuary 14, 1994
K925755DE LUXEDecember 3, 1993
K925756UNI IIOctober 18, 1993