Medical Device Manufacturer · US , Mundelein , IL

Douglas Medical Products Corp. - FDA 510(k) Cleared Devices

19 submissions · 19 cleared · Since 1992

Total

Cleared

Denied

Douglas Medical Products Corp. has 19 FDA 510(k) cleared general hospital devices. Based in Mundelein, US.

Historical record: 19 cleared submissions from 1992 to 1996.

Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Douglas Medical Products Corp.

19 devices

1-12 of 19

Cleared Jun 18, 1996

SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908

K961155 · LJS

General Hospital · 88d

Cleared Mar 28, 1996

SOLOPICC 24 (60CM) 20GA CATHETER

K954428 · FOZ

General Hospital · 188d

Cleared Feb 16, 1995

40 MICRON BLOOD TRANSFUSION FILTER

K941628 · FPB

General Hospital · 318d

Cleared Sep 30, 1994

4-LEAD IRRIGATION SET

K942101 · HRX

Orthopedic · 151d

Cleared Aug 16, 1994

CHECK VALVE SOLUTION SET

K941453 · FPA

General Hospital · 144d

Cleared Jan 14, 1994

SOLUTION SET WITH .2 MICRON FILTER

K930854 · FPA

General Hospital · 330d

Cleared Jan 07, 1994

3 LEAD CONNECTOR

K931659 · FPA

General Hospital · 277d

Cleared Jan 07, 1994

SUBCUTANEOUS INFUSION SET

K932637 · FPA

General Hospital · 219d

Cleared Dec 21, 1993

IN-LINE BURETTE SET

K931658 · FPA

General Hospital · 260d

Cleared Dec 14, 1993

HUBER NEEDLE INFUSION SET

K932638 · FPA

General Hospital · 195d

Cleared Nov 10, 1993

EVA EMPTY MIXING CONTAINER

K932640 · KPE

General Hospital · 161d

Cleared Nov 10, 1993

EMPTY MIXING CONTAINER

K932641 · KPE

General Hospital · 161d

Douglas Medical Products Corp. - FDA 510(k) Cleared Devices

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