Medical Device Manufacturer · US , Mchenry , IL

Sage Products, Inc. - FDA 510(k) Cleared Devices

31 submissions · 30 cleared · Since 1978

Total

Cleared

Denied

Sage Products, Inc. has 30 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 30 cleared submissions from 1978 to 1998. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Sage Products, Inc.

31 devices

1-12 of 31

Cleared Apr 30, 1998

RESHEATHER DEVICE-METAL OR PLASTIC, RESHEATER/ NEEDLE HOLDER DEVICE-PLASTIC

K972705 · FMI

General Hospital · 283d

Cleared Feb 24, 1998

SAGE PRODUCTS INC, SHARPS DISPOSAL CONTAINERS WITH SCREW TOP CAPS

K980490 · MMK

General Hospital · 15d

Cleared Oct 29, 1997

2 GALLON ALTERNATE CARE SHARPS CONTAINER

K973911 · FMI

General Hospital · 15d

Cleared Aug 29, 1997

SHARPS SHUTTLE

K972279 · FMI

General Hospital · 72d

Cleared Aug 25, 1997

NITRILE GLOVES

K970135 · LZC

General Hospital · 222d

Cleared Jul 25, 1997

POCKET COUNT OR SAFETCOUNT

K972302 · LWH

General & Plastic Surgery · 36d

Cleared Mar 03, 1997

PROCEDURE SPECIFIC KITS

K964168 · FXX

General Hospital · 137d

Cleared Nov 08, 1996

STP SYSTEM PVA WITH ZINC

STP SYSTEM-PVA WITH MERCURY

General Hospital · 47d

Cleared Mar 22, 1995

CHEMOTHERAPY WASTE DISPOSAL CONTAINERS

K943658 · MMK

General Hospital · 238d

Sage Products, Inc. - FDA 510(k) Cleared Devices

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