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

NORCATH VASCULAR ACCESS CATHETERS

K Number: K911067 · Decision Jun 3, 1991
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
301
Applicant Total
4
Review Days
84

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Basic Information

Device Name
NORCATH VASCULAR ACCESS CATHETERS
K Number
K911067
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5970
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Norfolk Medical
Date Received
March 11, 1991
Decision Date
June 3, 1991
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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K905646 OMEGAPORT SUBCUTANEOUSLY IMPLANTED DRUG DELIVERY