FDA 510(k) FDA unclassified Substantially Equivalent 🇩🇪 Germany

COSP2

K Number: K093721 · Decision Feb 19, 2010
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
35
Applicant Total
24
Review Days
79

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Basic Information

Device Name
COSP2
K Number
K093721
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
3M Espe AG Dental Products
Date Received
December 2, 2009
Decision Date
February 19, 2010
Product Code
MVL
Advisory Committee
Unknown
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MVL Cord, Retraction

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