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

NEEDLELESS INJECTION CANNULA

K Number: K923653 · Decision May 13, 1993
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
297
Applicant Total
110
Review Days
296

Basic Information

Device Name
NEEDLELESS INJECTION CANNULA
K Number
K923653
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5970
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ARROW INTL., INC.
Date Received
July 21, 1992
Decision Date
May 13, 1993
Product Code
LJS
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

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