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 |