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

TEMP. REPAIR KIT-DUAL LUMEN CATHETER

K Number: K831587 · Decision Oct 19, 1983
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
301
Applicant Total
39
Review Days
155

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Basic Information

Device Name
TEMP. REPAIR KIT-DUAL LUMEN CATHETER
K Number
K831587
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5970
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Norton Performance Plastics Corp.
Date Received
May 17, 1983
Decision Date
October 19, 1983
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LJS), ordered by most recent decision date.

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Other Clearances by Norton Performance Plastics Corp.

K Number Device Name
K853791 NORTON CARDIOPLEGIC QUICK COOLING COIL 421738-000
K852914 ANGIOGRAPHIC, WEDGE PRESS, DUAL THERMOD & INFUSION
K851299 CORRECT FLO
K842858 FLUID ADMINISTRATION LINE W/SPIKE 14-923
K841828 CENTRAL VENOUS CATHETER W/BIG-GARD
K840240 MICROFUSE INTRAVENOUS CATHETER SET
K831698 DISPOSABLE PRESSURE TRANSDUCER#14004195
K830788 CENTRAL VEIN CATHERIZATION KIT-14-690-
K830813 FRENCH PERCUTANEOUS SHEATH INTRODUCER
K830969 PERM. REPAIR KIT FOR LEONARD NORTON DUAL
Search all 39 clearances from Norton Performance Plastics Corp. →