FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇰 Denmark

INTUITION INFUSION SETS

K Number: K061374 · Decision Jul 31, 2006
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
13
Review Days
75

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Basic Information

Device Name
INTUITION INFUSION SETS
K Number
K061374
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Unomedical A/S
Date Received
May 17, 2006
Decision Date
July 31, 2006
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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K Number Device Name
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K160648 MiniMed Quick-Set® MiniMed Sure-T® MiniMed Silhouette® MiniMed Mio®
K132142 NERIA SOFT 90 INFUSION SET
K120337 I-PORT ADVANCE INJECTION PORT
K070430 PARADIGM QUICK-SET II AND QUICK-SET II SUBCUTANEOUS INFUSION SETS
K051264 COMFORT AND INSET SUBCUTANEOUS INFUSION SETS FOR USE WITH ABBOTT INFUSION PUMPS
K041545 CONTACT DETACH
Search all 13 clearances from Unomedical A/S →