ANGIO-FLO
Catheter, Continuous Flush
DESERET MEDICAL, INC.
The following data is part of a premarket notification filed by Deseret Medical, Inc. with the FDA for Angio-flo.
Pre-market Notification Details
| Device ID | K790327 |
| 510k Number | K790327 |
| Device Name: | ANGIO-FLO |
| Classification | Catheter, Continuous Flush |
| Applicant | DESERET MEDICAL, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KRA |
| CFR Regulation Number | 870.1210 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-02-16 |
| Decision Date | 1979-02-26 |
Trademark Results [ANGIO-FLO]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ANGIO-FLO 73229672 1141243 Dead/Cancelled |
Deseret Company, The 1979-08-30 |
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