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

NIPRO DISPOSABLE SOLUTION INFUSION SET

K Number: K972493 · Decision Sep 18, 1997
Classifications
1
FEI Numbers
437
Registration Numbers
437
Same Product Code
1167
Applicant Total
27
Review Days
77

Basic Information

Device Name
NIPRO DISPOSABLE SOLUTION INFUSION SET
K Number
K972493
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NIPRO MEDICAL CORP.
Date Received
July 3, 1997
Decision Date
September 18, 1997
Product Code
FPA
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
FPA Set, Administration, Intravascular

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Other Clearances by NIPRO MEDICAL CORP.

K Number Device Name
K093985 NIPRO SAFETOUCH LOCKTAIL SAFETY FISTULA NEEDLE
K081210 NIPRO SAFETOUCH HUBER INFUSTION SET
K072024 NIPRO BLOOD TUBING SET WITH TRANSDUCER PROTECTOR AND PRIMING SET, MODEL A201-A219, V801-V806, 5M9634, 5M9693
K063368 NIPRO BIOHOLE NEEDLE
K063721 NIPRO SAFETOUCH II GAMMA
K052474 NIPRO HYPODERMIC NEEDLE
K051574 NIPRO DISPOSABLE SYRINGE WITH OR WITHOUT NEEDLE
K041779 NIPRO DISPOSABLE STOPCOCKS, MODELS 3W-RC. NCN-3, 3W-R, 3W-L
K032777 MODIFICATION TO: NIPRO SAFE TOUCH SAFETY FISTULA NEEDLE
K030683 NIPRO DISPOSABLE SYRINGES
Search all 27 clearances from NIPRO MEDICAL CORP. →