Medical Device Manufacturer · US , Versailles , OH

Midmark Corp. - FDA 510(k) Cleared Devices

31 submissions · 31 cleared · Since 1981

31

Total

31

Cleared

0

Denied

FDA 510(k) Regulatory Record - Midmark Corp. General Hospital ✕

16 devices

1-12 of 16

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 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 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

Cleared Aug 26, 1991

MODEL #M9 ULTRACLAVE STEAM STERILIZER

General Hospital · 153d

Cleared Oct 03, 1990

MODEL #527 OPHTHALMIC STRETCHER

General Hospital · 35d

Cleared Jul 27, 1990

MODEL #M8 ELECTRONIC STERILIZER

General Hospital · 178d

Cleared Sep 12, 1989

MODEL #535 PACU STRETCHER/BED & #530 ED/TRAUMA STR

General Hospital · 60d

Cleared Aug 28, 1989

POWER EXAMINATION TABLE MODEL # 411

General Hospital · 76d