FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

MEDCOMP PERITONEAL DIALYSIS CATHETERS

K Number: K915490 · Decision Feb 2, 1994
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
47
Applicant Total
63
Review Days
789

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Basic Information

Device Name
MEDCOMP PERITONEAL DIALYSIS CATHETERS
K Number
K915490
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5630
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Summary
Applicant
Medical Components, Inc.
Date Received
December 6, 1991
Decision Date
February 2, 1994
Product Code
FJS
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
FJS Catheter, Peritoneal, Long-Term Indwelling

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K Number Device Name
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K132880 MEDCOMP POWER INJECTABLE SAFETY HUBER NEEDLE
K131687 6F X 60CM TRIPLE PRO-LINE CT BASIC IR SET
K130687 2F & 3F VASCU-SHEATH TEARAWAY INTRODUCER
K130923 5F DIGNITY CT TITANIUM PORT
K124046 VALVED TEARAWAY INTRODUCER GENERATION II
K123617 3F PRO-PICC
K122423 VASU-PICC
K121848 SPLIT CATH III 24CM SPLIT CATH III 24CM SPLIT CATH III 32CM CATH III 36CM SPLIT CATH III 40CM AND 55CM
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