The following data is part of a premarket notification filed by Kingswood Laboratories, Inc. with the FDA for Moi-stir.
Device ID | K810157 |
510k Number | K810157 |
Device Name: | MOI-STIR |
Classification | Saliva, Artificial |
Applicant | KINGSWOOD LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | LFD |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1981-01-21 |
Decision Date | 1981-02-10 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00355299601040 | K810157 | 000 |
00304369600421 | K810157 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MOI-STIR 87347864 5290448 Live/Registered |
Century Pharmaceuticals, Inc. 2017-02-23 |
![]() MOI-STIR 78911158 3334982 Live/Registered |
Century Pharmaceuticals, Inc. 2006-06-19 |
![]() MOI-STIR 73188328 1206885 Dead/Cancelled |
Kingswood Laboratories, Inc. 1979-12-03 |