The following data is part of a premarket notification filed by Mrlb Intl., Inc. with the FDA for Dentapure Dp40 Cartridge.
Device ID | K992868 |
510k Number | K992868 |
Device Name: | DENTAPURE DP40 CARTRIDGE |
Classification | Unit, Operative Dental |
Applicant | MRLB INTL., INC. 2450 COLLEGE WAY Fergus Falls, MN 56537 |
Contact | B.j. Hammarback |
Correspondent | B.j. Hammarback MRLB INTL., INC. 2450 COLLEGE WAY Fergus Falls, MN 56537 |
Product Code | EIA |
CFR Regulation Number | 872.6640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-08-26 |
Decision Date | 1999-09-07 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10732224005529 | K992868 | 000 |
00732224005522 | K992868 | 000 |