The following data is part of a premarket notification filed by Medikeeper, Inc. with the FDA for Medikeeper.
| Device ID | K912346 |
| 510k Number | K912346 |
| Device Name: | MEDIKEEPER |
| Classification | Cabinet, Table And Tray, Anesthesia |
| Applicant | MEDIKEEPER, INC. P.O.BOX 18692 Philadelphia, PA 19133 |
| Contact | David Sherman |
| Correspondent | David Sherman MEDIKEEPER, INC. P.O.BOX 18692 Philadelphia, PA 19133 |
| Product Code | BRY |
| CFR Regulation Number | 868.6100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-05-28 |
| Decision Date | 1991-07-30 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MEDIKEEPER 78620890 3082617 Dead/Cancelled |
MEDIKEEPER, INC. 2005-05-02 |