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

MODIFICATION TO TEMNO BIOPSY NEEDLES

K Number: K024120 · Decision Jan 15, 2003
Classifications
1
FEI Numbers
128
Registration Numbers
128
Same Product Code
132
Applicant Total
63
Review Days
30

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Basic Information

Device Name
MODIFICATION TO TEMNO BIOPSY NEEDLES
K Number
K024120
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Allegiance Healthcare Corp.
Date Received
December 16, 2002
Decision Date
January 15, 2003
Product Code
FCG
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
FCG Biopsy Needle

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K Number Device Name
K023673 AIRLIFE DEMAND NASAL CANNULA
K023419 TRILAMINATE DRAPES/TIBURON
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
K020818 POWDER-FREE LATEX EXAMINATION GLOVES WITH COLORANTS
Search all 63 clearances from Allegiance Healthcare Corp. →