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

DIMENSION PENTA H, DIMENSION PENTA H QUICK

K Number: K000591 · Decision Mar 30, 2000
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
401
Applicant Total
29
Review Days
37

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Basic Information

Device Name
DIMENSION PENTA H, DIMENSION PENTA H QUICK
K Number
K000591
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Espe Dental AG
Date Received
February 22, 2000
Decision Date
March 30, 2000
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 Espe Dental AG

K Number Device Name
K011394 LAVA FRAME, LAVA FRAME SHADE, LAVA CERAM
K011154 ELIPAR FREELIGHT
K002793 KETAC CEM U
K002364 PROTEMP H
K001494 MODIFICATION TO PROMPT L-POP
K000595 DIMENSION PENTA L
K000588 DIMENSION GARANT L, DIMENSION GARANT L QUICK
K994193 IMPREGUM PENTA DUOSOFT
K994192 IMPREGUM PENTA M MONOSOFT
K994190 IMPREGUM GARANT L DUOSOFT
Search all 29 clearances from Espe Dental AG →