The following data is part of a premarket notification filed by Dmp Ltd with the FDA for Bonasil A+ Impression Materials.
Device ID | K102836 |
510k Number | K102836 |
Device Name: | BONASIL A+ IMPRESSION MATERIALS |
Classification | Material, Impression |
Applicant | DMP LTD 2ND KM KALYVION AVENUE MARKOPOULO INDUSTRIAL ZONE Markopoulo, GR 19003 |
Contact | Dimitris Prantsidis |
Correspondent | Dimitris Prantsidis DMP LTD 2ND KM KALYVION AVENUE MARKOPOULO INDUSTRIAL ZONE Markopoulo, GR 19003 |
Product Code | ELW |
CFR Regulation Number | 872.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-09-29 |
Decision Date | 2011-01-13 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
20843471153875 | K102836 | 000 |
10843471152949 | K102836 | 000 |
20843471152939 | K102836 | 000 |
10843471152925 | K102836 | 000 |
10843471152918 | K102836 | 000 |
20843471152908 | K102836 | 000 |
10843471152895 | K102836 | 000 |
10843471152888 | K102836 | 000 |
10843471147679 | K102836 | 000 |
10843471152956 | K102836 | 000 |
10843471152963 | K102836 | 000 |
20843471153868 | K102836 | 000 |
10843471153854 | K102836 | 000 |
20843471153844 | K102836 | 000 |
20843471153837 | K102836 | 000 |
20843471153820 | K102836 | 000 |
20843471153813 | K102836 | 000 |
10843471153809 | K102836 | 000 |
20843471152977 | K102836 | 000 |
10840326406912 | K102836 | 000 |