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

MEDTRONIC MINIMED SOF-SITE INFUSION SET, MODELS MMT-358S6, MMT-358M6, MMT-358L6, MMT-358S9, MMT-358M9, AND MMT-358L9

K Number: K030137 · Decision Feb 19, 2003
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
5
Review Days
36

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Basic Information

Device Name
MEDTRONIC MINIMED SOF-SITE INFUSION SET, MODELS MMT-358S6, MMT-358M6, MMT-358L6, MMT-358S9, MMT-358M9, AND MMT-358L9
K Number
K030137
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Avail Medical Products, Inc.
Date Received
January 14, 2003
Decision Date
February 19, 2003
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 Avail Medical Products, Inc.

K Number Device Name
K112209 PREFILLED CATHETER INFLATION SYRINGE
K090121 PRE-FILLED CATHETER INFLATION SYRINGE
K083189 STERI-LUB LUBRICATION GEL
K030149 MEDTRONIC MINIMED SOF-SITE INFUSION SET, MODELS MMT-359S6, MMT-359M6, MMT-359L6, MMT-359S9, MMT-359M9, AND MMT-359L9