The following data is part of a premarket notification filed by Norton Performance Plastics Corp. with the FDA for Single, 2&3 Way Solution Sets #14-070 Et.
| Device ID | K800618 |
| 510k Number | K800618 |
| Device Name: | SINGLE, 2&3 WAY SOLUTION SETS #14-070 ET |
| Classification | Catheter, Intravascular, Diagnostic |
| Applicant | NORTON PERFORMANCE PLASTICS CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DQO |
| CFR Regulation Number | 870.1200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-03-18 |
| Decision Date | 1980-04-24 |