Midmark Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Midmark Corp. - FDA 510(k) Cleared Devices
Recent clearances: VANTAGE MODEL V5000, V5100, V5000C, V5100C, CLEARVISION, MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZER
31
Total
31
Cleared
0
Denied
Midmark Corp. has 31 FDA 510(k) cleared medical devices. Based in Versailles, US.
Historical record: 31 cleared submissions from 1981 to 2013. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Midmark Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Midmark Corp.
31 devices
Cleared
Jan 07, 2013
VANTAGE MODEL V5000, V5100, V5000C, V5100C
Radiology
131d
Cleared
Nov 22, 2011
CLEARVISION
Radiology
97d
Cleared
Jul 07, 2009
MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZER
General Hospital
116d
Cleared
Mar 03, 2003
MIDMARK M9 ULTRACLAVE STEAM STERILIZER
General Hospital
147d
Cleared
Oct 18, 2000
MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM
Dental
15d
Cleared
Jan 10, 2000
MIDMARK M4*9 EASYCLAVE STEAM STERILIZER
General Hospital
147d
Cleared
Apr 19, 1999
MODIFICATION OF: MIDMARK M-11 ULTRACLAVE STEAM STERILIZER
General Hospital
89d
Cleared
Nov 30, 1994
MIDMARK M-11 ULTRACLAVE STEAM STERILIZER
General Hospital
338d
Cleared
Oct 21, 1994
RITTERMODEL 75 EVOLUTION UNIV POW EXAM TABLE/ACCES
General & Plastic Surgery
666d
Cleared
Mar 28, 1994
MIDMARK MAGNUM GENERAL SURGICAL TABLE
General & Plastic Surgery
175d
Cleared
Feb 09, 1994
MODEL 561 C-ARM PROCEDURES STRETCHER
General Hospital
562d
Cleared
Dec 02, 1993
RITTER MODEL 158 AND 159 EXAM LIGHTS
General Hospital
181d