Medical Device Manufacturer · US , Versailles , OH

Midmark Corp. - FDA 510(k) Cleared Devices

31 submissions · 31 cleared · Since 1981

Total

Cleared

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.

FDA 510(k) Regulatory Record - Midmark Corp.

31 devices

1-12 of 31

Cleared Jan 07, 2013

VANTAGE MODEL V5000, V5100, V5000C, V5100C

MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZER

K090670 · FLE

General Hospital · 116d

Cleared Mar 03, 2003

MIDMARK M9 ULTRACLAVE STEAM STERILIZER

K023348 · FLE

General Hospital · 147d

Cleared Oct 18, 2000

MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM

K003090 · EIA

Dental · 15d

Cleared Jan 10, 2000

MIDMARK M4*9 EASYCLAVE STEAM STERILIZER

K992744 · FLE

General Hospital · 147d

Cleared Apr 19, 1999

MODIFICATION OF: MIDMARK M-11 ULTRACLAVE STEAM STERILIZER

K990189 · FLE

General Hospital · 89d

Cleared Nov 30, 1994

MIDMARK M-11 ULTRACLAVE STEAM STERILIZER

K936181 · FLE

General Hospital · 338d

Cleared Oct 21, 1994

RITTERMODEL 75 EVOLUTION UNIV POW EXAM TABLE/ACCES

K926463 · FQO

General & Plastic Surgery · 666d

Cleared Mar 28, 1994

MIDMARK MAGNUM GENERAL SURGICAL TABLE

K934744 · GDC

General & Plastic Surgery · 175d

Cleared Feb 09, 1994

MODEL 561 C-ARM PROCEDURES STRETCHER

K923730 · FPO

General Hospital · 562d

Cleared Dec 02, 1993

RITTER MODEL 158 AND 159 EXAM LIGHTS

K932719 · KZF

General Hospital · 181d

Midmark Corp. - FDA 510(k) Cleared Devices

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