KINNET
Bed, Patient Rotation, Manual
KINETIC CONCEPTS, INC.
The following data is part of a premarket notification filed by Kinetic Concepts, Inc. with the FDA for Kinnet.
Pre-market Notification Details
| Device ID | K851875 |
| 510k Number | K851875 |
| Device Name: | KINNET |
| Classification | Bed, Patient Rotation, Manual |
| Applicant | KINETIC CONCEPTS, INC. 4958 STOUT DR. San Antonio, TX 78219 |
| Contact | Robert A Nehrmeyer |
| Correspondent | Robert A Nehrmeyer KINETIC CONCEPTS, INC. 4958 STOUT DR. San Antonio, TX 78219 |
| Product Code | INY |
| CFR Regulation Number | 890.5180 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-04-29 |
| Decision Date | 1985-08-22 |
Trademark Results [KINNET]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 KINNET 87218680 5259590 Live/Registered |
aihong,huang 2016-10-28 |
 KINNET 74356982 1795303 Dead/Cancelled |
KIN Network, Inc. 1993-02-09 |
 KINNET 73683040 not registered Dead/Abandoned |
KINETIC CONCEPTS, INC. 1987-09-08 |
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