Midmark Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
33
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K122643VANTAGE MODEL V5000, V5100, V5000C, V5100CJanuary 7, 2013
K120239ELEVANCEAugust 24, 2012
K112380CLEARVISIONNovember 22, 2011
K091866PROGENY VANTAGE PANORAMIC X-RAY SYSTEMJuly 20, 2009
K090670MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZERJuly 7, 2009
K023348MIDMARK M9 ULTRACLAVE STEAM STERILIZERMarch 3, 2003
K003090MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEMOctober 18, 2000
K992744MIDMARK M4*9 EASYCLAVE STEAM STERILIZERJanuary 10, 2000
K990189MODIFICATION OF: MIDMARK M-11 ULTRACLAVE STEAM STERILIZERApril 19, 1999
K936181MIDMARK M-11 ULTRACLAVE STEAM STERILIZERNovember 30, 1994
K926463RITTERMODEL 75 EVOLUTION UNIV POW EXAM TABLE/ACCESOctober 21, 1994
K934744MIDMARK MAGNUM GENERAL SURGICAL TABLEMarch 28, 1994
K923730MODEL 561 C-ARM PROCEDURES STRETCHERFebruary 9, 1994
K932719RITTER MODEL 158 AND 159 EXAM LIGHTSDecember 2, 1993
K930686MIDMARK SURGICAL LIGHTING SYSTEMSJuly 30, 1993
K915141712 PLASTIC SURGERY TABLE & ACCESORIESJanuary 9, 1992
K911322MODEL #M9 ULTRACLAVE STEAM STERILIZERAugust 26, 1991
K910781#491 POWER OTOLARYNGOLY CH/#498 PROCED CTR & ACCESMay 15, 1991
K904011MODEL #527 OPHTHALMIC STRETCHEROctober 3, 1990
K900432MODEL #M8 ELECTRONIC STERILIZERJuly 27, 1990