Medical Device Manufacturer · US , Mchenry , IL

Devon Industries, Inc. - FDA 510(k) Cleared Devices

47 submissions · 46 cleared · Since 1976

Total

Cleared

Denied

Devon Industries, Inc. has 46 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 46 cleared submissions from 1976 to 1996. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Devon Industries, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Devon Industries, Inc.

47 devices

1-12 of 47

Cleared Jul 03, 1996

BIRTHDAY KIT (OBSTETRICAL DELIVERY KIT)

K961993 · MLS

Obstetrics & Gynecology · 43d

Cleared Nov 20, 1995

ABG POINT LOK NEEDLE PROTECTION DEVICE

K954015 · CBT

Anesthesiology · 87d

Cleared Jul 10, 1995

DEVONS POINT LOK NEEDLE PROTECTION DEVICE

K946289 · FMI

General Hospital · 195d

Cleared Dec 02, 1994

POINT OF USE SHARPS A GATOR

K943892 · FMI

General Hospital · 115d

Cleared Dec 02, 1994

PHLEBOTOMY UNIT SHARPS A GATOR

K944114 · FMI

General Hospital · 101d

Cleared Dec 02, 1994

THE SHARPS COLLECTION AND DISPOSAL SYSTEM

K945197 · MMK

General Hospital · 39d

Cleared Nov 29, 1994

ABG NEEDLE PROTECTION

General & Plastic Surgery · 61d

Cleared Aug 26, 1991

DEVON SPONGE COUNTER BAGS

K912824 · LWH

General & Plastic Surgery · 61d

Cleared Sep 07, 1989

DEVON DISPOSABLE HEAD POSITIONER COVER

K894170 · KME

General Hospital · 84d

Cleared Aug 15, 1989

HIBERNATION KIT

K892660 · CAZ

Anesthesiology · 124d

Cleared Apr 10, 1987

SURGICAL STARTER KIT

K870744

General & Plastic Surgery · 44d

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Devon Industries, Inc. - FDA 510(k) Cleared Devices

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