The following data is part of a premarket notification filed by Warner-lambert Co. with the FDA for Deseret Intracath Intravenous Catheter.
| Device ID | K821372 |
| 510k Number | K821372 |
| Device Name: | DESERET INTRACATH INTRAVENOUS CATHETER |
| Classification | Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days |
| Applicant | WARNER-LAMBERT CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FOZ |
| CFR Regulation Number | 880.5200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-05-10 |
| Decision Date | 1982-06-02 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20886333210163 | K821372 | 000 |
| 20886333210156 | K821372 | 000 |
| 20886333210149 | K821372 | 000 |
| 20886333210132 | K821372 | 000 |
| 20886333210125 | K821372 | 000 |
| 20886333210118 | K821372 | 000 |
| 20886333210101 | K821372 | 000 |