The following data is part of a premarket notification filed by Parke-davis Co. with the FDA for Intracath-da Intravenous Cath. Placement.
| Device ID | K823064 |
| 510k Number | K823064 |
| Device Name: | INTRACATH-DA INTRAVENOUS CATH. PLACEMENT |
| Classification | Catheter, Intravascular, Diagnostic |
| Applicant | PARKE-DAVIS CO. 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 | 1982-10-18 |
| Decision Date | 1983-01-27 |