Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K001414
Device Classification Name
Material, Impression
More FDA Info for this Device
510(K) Number
K001414
Device Name
Material, Impression
Applicant
R-DENTAL DENTALERZEUGNISSE GMBH
WINTERHUDER WEG 88
HAMBURG D-22085 DE
Other 510(k) Applications for this Company
Contact
ANDREAS SPRAFKE
Other 510(k) Applications for this Contact
Regulation Number
872.3660
More FDA Info for this Regulation Number
Classification Product Code
ELW
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/04/2000
Decision Date
08/09/2000
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact