The following data is part of a premarket notification filed by Neurocom International, Inc. with the FDA for Dual Forceplate.
| Device ID | K863443 |
| 510k Number | K863443 |
| Device Name: | DUAL FORCEPLATE |
| Classification | Platform, Force-measuring |
| Applicant | NEUROCOM INTERNATIONAL, INC. 2326 NW LOVEJOY ST. P.O. BOX 12529 Portland, OR 97210 |
| Contact | Jack Kelly |
| Correspondent | Jack Kelly NEUROCOM INTERNATIONAL, INC. 2326 NW LOVEJOY ST. P.O. BOX 12529 Portland, OR 97210 |
| Product Code | KHX |
| CFR Regulation Number | 890.1575 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-09-05 |
| Decision Date | 1986-09-17 |