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

CLEAR HUB SPINAL NEEDLE 14GA, 16GA, 17GA, 18GA, 20GA, 21GA, 22GA, 25GA, 26GA AND 27GA

K Number: K982269 · Decision Jul 23, 1998
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
9
Applicant Total
63
Review Days
24

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Basic Information

Device Name
CLEAR HUB SPINAL NEEDLE 14GA, 16GA, 17GA, 18GA, 20GA, 21GA, 22GA, 25GA, 26GA AND 27GA
K Number
K982269
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5150
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Allegiance Healthcare Corp.
Date Received
June 29, 1998
Decision Date
July 23, 1998
Product Code
MIA
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
MIA Needle, Spinal, Short Term

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Other Clearances by Allegiance Healthcare Corp.

K Number Device Name
K023673 AIRLIFE DEMAND NASAL CANNULA
K023419 TRILAMINATE DRAPES/TIBURON
K024120 MODIFICATION TO TEMNO BIOPSY NEEDLES
K024292 MODIFICATION TO POSITIVE TOUCH POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN AND CHEMOTHERAPY LABELING CLAIM
K024102 DENTAL POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN LABELING CLAIM
K023425 DRAPES WITH ABSORBENT REINFORCEMENT
K022765 NITRILE POWDER-FREE EXAMINATION GLOVES
K023170 NITRILE POWDER-FREE EXAMINATION GLOVES
K023167 BREATHABLE SURGICAL GOWN
K012931 GENESIS STERRAD COMPATIBLE REUSABLE STERILIZATION CONTAINER SYSTEM
Search all 63 clearances from Allegiance Healthcare Corp. →