Medical Device Manufacturer · US , Skokie , IL

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

39 submissions · 38 cleared · Since 1988

Total

Cleared

Denied

Manan Medical Products, Inc. has 38 FDA 510(k) cleared medical devices. Based in Skokie, US.

Historical record: 38 cleared submissions from 1988 to 2005. Primary specialty: Gastroenterology & Urology.

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

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

39 devices

1-12 of 39

Cleared Nov 01, 2005

MANAN BIO-CUT SOFT TISSUE BIOPSY NEEDLE

K052802 · KNW

Gastroenterology & Urology · 29d

Cleared Jun 26, 2001

MANAN SPRITACRE SPINAL NEEDLES

Anesthesiology · 170d

Cleared Jun 29, 1998

MANAN BLUNT NEEDLE

K981386 · FPA

General Hospital · 74d

Cleared Feb 06, 1998

MRI CHIBA,SPINAL,BREAST LOCALIZATION,AUTOMATIC CUTTING NEEDLES

K980211 · KNW

Gastroenterology & Urology · 16d

Cleared Jan 08, 1998

MANAN AUTOMATIC CUTTING NEEDLE

K974446 · KNW

Gastroenterology & Urology · 44d

Cleared Oct 09, 1997

MRI COMPATIBLE BIOPSY NEEDLES

K962977 · KNW

Gastroenterology & Urology · 435d

Cleared May 16, 1997

MANAN V.S. ACCESS NEEDLE/SET

K963767 · FGE

Gastroenterology & Urology · 239d

Cleared Mar 13, 1997

MANAN D BAG

K961986 · EXF

Gastroenterology & Urology · 296d

Cleared Jan 10, 1997

MANAN PEDIATRIC BONE MARROW ACCESS NEEDLE

K962001 · FMI

General Hospital · 233d

Cleared Dec 13, 1996

MANAN D BAG

K963849 · EXF

Gastroenterology & Urology · 79d

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

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