The following data is part of a premarket notification filed by Deseret Medical, Inc. with the FDA for Angio-set Intravenous Cath. Set.
| Device ID | K833657 |
| 510k Number | K833657 |
| Device Name: | ANGIO-SET INTRAVENOUS CATH. SET |
| Classification | Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days |
| Applicant | DESERET MEDICAL, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | FOZ |
| CFR Regulation Number | 880.5200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-10-18 |
| Decision Date | 1983-12-27 |