FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MRI COMPATIBLE BIOPSY NEEDLES

K Number: K962977 · Decision Oct 9, 1997
Classifications
1
FEI Numbers
207
Registration Numbers
207
Same Product Code
360
Applicant Total
39
Review Days
435

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Basic Information

Device Name
MRI COMPATIBLE BIOPSY NEEDLES
K Number
K962977
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Manan Medical Products, Inc.
Date Received
July 31, 1996
Decision Date
October 9, 1997
Product Code
KNW
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KNW Instrument, Biopsy

Similar 510(k) Clearances

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Other Clearances by Manan Medical Products, Inc.

K Number Device Name
K052802 MANAN BIO-CUT SOFT TISSUE BIOPSY NEEDLE
K011209 MANAN SPRITACRE SPINAL NEEDLES
K983620 MANAN SPINAL NEEDLES
K980536 EPIDURAL NEEDLE
K981386 MANAN BLUNT NEEDLE
K980211 MRI CHIBA,SPINAL,BREAST LOCALIZATION,AUTOMATIC CUTTING NEEDLES
K974446 MANAN AUTOMATIC CUTTING NEEDLE
K963767 MANAN V.S. ACCESS NEEDLE/SET
K961986 MANAN D BAG
K962001 MANAN PEDIATRIC BONE MARROW ACCESS NEEDLE
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