The following data is part of a premarket notification filed by Nsk America Corp. with the FDA for Pana Spray Plus.
| Device ID | K131014 |
| 510k Number | K131014 |
| Device Name: | PANA SPRAY PLUS |
| Classification | Handpiece, Air-powered, Dental |
| Applicant | NSK AMERICA CORP. 1201 RICHARDSON DR. SUITE 280 Richardson, TX 75080 |
| Contact | Diane Rutherford |
| Correspondent | Diane Rutherford NSK AMERICA CORP. 1201 RICHARDSON DR. SUITE 280 Richardson, TX 75080 |
| Product Code | EFB |
| CFR Regulation Number | 872.4200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-04-11 |
| Decision Date | 2013-08-12 |
| Summary: | summary |