FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

POLYPERF / POLYPERF SAFE

K Number: K063631 · Decision Oct 5, 2007
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
1
Review Days
303

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Basic Information

Device Name
POLYPERF / POLYPERF SAFE
K Number
K063631
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Laboratoires Perouse
Date Received
December 6, 2006
Decision Date
October 5, 2007
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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