ARMBOARD
System, X-ray, Stationary
MTD, INC.
The following data is part of a premarket notification filed by Mtd, Inc. with the FDA for Armboard.
Pre-market Notification Details
| Device ID | K833559 |
| 510k Number | K833559 |
| Device Name: | ARMBOARD |
| Classification | System, X-ray, Stationary |
| Applicant | MTD, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KPR |
| CFR Regulation Number | 892.1680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-10-05 |
| Decision Date | 1984-01-03 |
Trademark Results [ARMBOARD]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ARMBOARD 77513027 3617405 Dead/Cancelled |
2Hinnovations 2008-07-01 |
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