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

PROCEM

K Number: K984248 · Decision Jan 8, 1999
Classifications
1
FEI Numbers
142
Registration Numbers
142
Same Product Code
495
Applicant Total
29
Review Days
42

Basic Information

Device Name
PROCEM
K Number
K984248
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ESPE DENTAL AG
Date Received
November 27, 1998
Decision Date
January 8, 1999
Product Code
EMA
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
EMA Cement, Dental

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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
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