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

TRIMPORT

K Number: K942623 · Decision Aug 23, 1994
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
285
Applicant Total
8
Review Days
88

Basic Information

Device Name
TRIMPORT
K Number
K942623
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5965
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
GERARD MEDICAL ENTERPRISES, INC.
Date Received
May 27, 1994
Decision Date
August 23, 1994
Product Code
LJT
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
LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

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K912111 MODIFIED VERSION IMPLANTABLE VASCULAR ACCESS SYSTE
K903364 GERARD MEDICAL, INC. TRIM-PORT
K813358 GERARD MEDICAL ELECTRODE TESTER