FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

PROTEMP H

K Number: K002364 · Decision Aug 10, 2000
Classifications
1
FEI Numbers
180
Registration Numbers
180
Same Product Code
188
Applicant Total
29
Review Days
7

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Basic Information

Device Name
PROTEMP H
K Number
K002364
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.3770
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Espe Dental AG
Date Received
August 3, 2000
Decision Date
August 10, 2000
Product Code
EBG
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
EBG Crown And Bridge, Temporary, Resin

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K Number Device Name
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K002793 KETAC CEM U
K001494 MODIFICATION TO PROMPT L-POP
K000595 DIMENSION PENTA L
K000588 DIMENSION GARANT L, DIMENSION GARANT L QUICK
K000591 DIMENSION PENTA H, DIMENSION PENTA H QUICK
K994193 IMPREGUM PENTA DUOSOFT
K994192 IMPREGUM PENTA M MONOSOFT
K994190 IMPREGUM GARANT L DUOSOFT
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