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

MODIFICATION OF PROMPT L-POP

K Number: K992048 · Decision Aug 16, 1999
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
418
Applicant Total
29
Review Days
60

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Basic Information

Device Name
MODIFICATION OF PROMPT L-POP
K Number
K992048
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Espe Dental AG
Date Received
June 17, 1999
Decision Date
August 16, 1999
Product Code
KLE
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
KLE Agent, Tooth Bonding, Resin

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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
K000591 DIMENSION PENTA H, DIMENSION PENTA H QUICK
K994193 IMPREGUM PENTA DUOSOFT
K994192 IMPREGUM PENTA M MONOSOFT
Search all 29 clearances from Espe Dental AG →