Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K190571
Device Classification Name
Material, Impression
More FDA Info for this Device
510(K) Number
K190571
Device Name
Material, Impression
Applicant
Dreve Dentamid GmbH
Max-Planck-Strasse 31
Unna 59423 DE
Other 510(k) Applications for this Company
Contact
Reiner Altmann
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
03/06/2019
Decision Date
11/07/2019
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact