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

MANAN SPINAL NEEDLES

K Number: K983620 · Decision Jan 8, 1999
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
151
Applicant Total
39
Review Days
85

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Basic Information

Device Name
MANAN SPINAL NEEDLES
K Number
K983620
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5150
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Manan Medical Products, Inc.
Date Received
October 15, 1998
Decision Date
January 8, 1999
Product Code
BSP
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BSP Needle, Conduction, Anesthetic (W/Wo Introducer)

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
K980536 EPIDURAL NEEDLE
K981386 MANAN BLUNT NEEDLE
K980211 MRI CHIBA,SPINAL,BREAST LOCALIZATION,AUTOMATIC CUTTING NEEDLES
K974446 MANAN AUTOMATIC CUTTING NEEDLE
K962977 MRI COMPATIBLE BIOPSY NEEDLES
K963767 MANAN V.S. ACCESS NEEDLE/SET
K961986 MANAN D BAG
K962001 MANAN PEDIATRIC BONE MARROW ACCESS NEEDLE
Search all 39 clearances from Manan Medical Products, Inc. →