The following data is part of a premarket notification filed by Pacific Dental Corp. with the FDA for Spaceline Three Way Syringe.
| Device ID | K801686 |
| 510k Number | K801686 |
| Device Name: | SPACELINE THREE WAY SYRINGE |
| Classification | Unit, Syringe, Air And/or Water |
| Applicant | PACIFIC DENTAL CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | ECB |
| CFR Regulation Number | 872.4565 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-07-21 |
| Decision Date | 1980-08-04 |