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

FREEALGIN

K Number: K070700 · Decision Apr 25, 2007
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
399
Applicant Total
19
Review Days
43

Basic Information

Device Name
FREEALGIN
K Number
K070700
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ZHERMACK S.P.A.
Date Received
March 13, 2007
Decision Date
April 25, 2007
Product Code
ELW
Advisory Committee
Dental
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
ELW Material, Impression

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Other Clearances by ZHERMACK S.P.A.

K Number Device Name
K083739 HYDRORISE AND HYDROSYSTEM
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K073005 ELITE GLASS
K070677 COLORISE
K053619 COLORBITE
K050417 ELITE IMPLANT
K051424 HYDROGUM 5
K043118 HYDROGUM SOFT
K043131 TORPICALGIN
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