The following data is part of a premarket notification filed by Dlp, Inc. with the FDA for Cuatico Myelography Needles.
| Device ID | K813367 |
| 510k Number | K813367 |
| Device Name: | CUATICO MYELOGRAPHY NEEDLES |
| Classification | Needle, Aspiration And Injection, Disposable |
| Applicant | DLP, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GAA |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-11-30 |
| Decision Date | 1982-01-05 |