The following data is part of a premarket notification filed by Pin Dot Products, Inc. with the FDA for Pin Dot Growth/dial Links.
| Device ID | K913553 |
| 510k Number | K913553 |
| Device Name: | PIN DOT GROWTH/DIAL LINKS |
| Classification | Components, Wheelchair |
| Applicant | PIN DOT PRODUCTS, INC. 6001 GROSS POINT RD. Niles, IL 60648 -4027 |
| Product Code | KNN |
| CFR Regulation Number | 890.3920 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-08-09 |
| Decision Date | 1991-09-05 |