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

BALLARD MEDICAL PRODUCTS EPIDURAL AND SPINAL NEEDLES

K Number: K000495 · Decision Mar 28, 2000
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
151
Applicant Total
26
Review Days
42

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Basic Information

Device Name
BALLARD MEDICAL PRODUCTS EPIDURAL AND SPINAL NEEDLES
K Number
K000495
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5150
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ballard Medical Products
Date Received
February 15, 2000
Decision Date
March 28, 2000
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)

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Other Clearances by Ballard Medical Products

K Number Device Name
K030721 QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLE
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K013892 LUTZ NEEDLE
K993138 BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT
K990376 BALLARD MEDICAL PRODUCTS FACILETOME BOW STRING PAPILLOTOME
K982894 MIC-KEY GLOW PROFILE GASTROSTOMY REPLACEMENT KIT
K974630 72 HOUR USE TRACH CARE WITH MICROBAN
K964369 TRACH CARE SET WITH MICROBAN
K951533 EASI-LAV PEDIATRIC / ADULT GASTRIC LAVAGE KIT
K923487 BAL CATH
Search all 26 clearances from Ballard Medical Products →