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

POSITION PENTA, POSITION PENTA QUICK

K Number: K974231 · Decision Jan 29, 1998
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
399
Applicant Total
17
Review Days
78

Basic Information

Device Name
POSITION PENTA, POSITION PENTA QUICK
K Number
K974231
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ESPE GMBH & CO. KG.
Date Received
November 12, 1997
Decision Date
January 29, 1998
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 GMBH & CO. KG.

K Number Device Name
K973513 SINFONY DENTIN, OPAQUE-DENTIN, ENAMEL, ENAMEL MODIFIER, TRANSPARENT OPAL,SINFONY MAGIC MODIFIERS, SINFONY OPAQUER
K973262 KETAC-FIL APLICAP PLUS
K972892 CAVIT-LC
K963735 COJET SYSTEM
K963737 HYCEM APLICAP
K962428 EBS (ESPE BONDING SYSTEM)
K962440 PERTAC II/PERTAC II APLITIP
K962442 HYTAC APLITIP/HYTAC OSB
K960954 KETAC-MOLAR APLICAP
K960547 DIMENSION PENTA/DIMENSION GARANT L/POLYVINYL SILOXANE ADHESIVE
Search all 17 clearances from ESPE GMBH & CO. KG. →