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

MEDCOMP REPAIR KIT, MODEL ASPCRPK

K Number: K022570 · Decision Oct 31, 2002
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
10
Applicant Total
40
Review Days
90

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Basic Information

Device Name
MEDCOMP REPAIR KIT, MODEL ASPCRPK
K Number
K022570
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5540
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medcomp
Date Received
August 2, 2002
Decision Date
October 31, 2002
Product Code
NFK
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
NFK Kit, Repair, Catheter, Hemodialysis

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K091586 VASCU-PICC AND MIDLINE CATHETERS, SINGLE, DOUBLE AND TRIPLE LUMEN
K091466 1.9F X 20CM VASCU-PICC, 1.9F X 50CM VASCU-PICC, MODEL VPI.9S20, VPI.9S50
K081775 THE MEDCOMP .010 VASCULAR GUIDEWIRES
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