Fresenius Hemoflow F6 and F8
FDA 510(k) K870725 · Seratronics, Inc.
510(k) numberK870725
Submission
- Device name
- Fresenius Hemoflow F6 and F8
- Applicant
- Seratronics, Inc.
Concord, CA, US - Received
- February 24, 1987
- Decision date
- May 1, 1987
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- FJI – Dialyzer, Capillary, Hollow Fiber
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.5820
- Specialty
- Gastroenterology, Urology
- Life-sustaining
- Yes
Other 510(k)s with product code FJI
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K190459 | Hemoflow F3 and F4 DialyzersFJI · Traditional | Fresenius Medical Care Renal Therapies Group, LLC | 08/23/2019SE |
| K122952 | Nipro Pureflux-L HemodialyzerFJI · Traditional | Nipro Medical Corporation | 12/04/2013SE |
| K043342 | Polyflux Family Hemodialyzer/Filter Labeled for Single and Multiple Use, Models 14L…FJI · Traditional | Gambro Renal Products | 05/27/2005SE |
| K010366 | Disposable Storage CapFJI · Abbreviated | Molded Products, Inc. | 11/28/2001SE |
| K011148 | Ultraconcentrator SystemFJI · Special | Interpore Cross Intl. | 06/13/2001SE |
| K002761 | Fresnius Hemoflow F7NR, F50NR, F70NR HemodialyzersFJI · Traditional | Fresenius Medical Care North America | 12/04/2000SE |
| K991908 | Idemsa Hemophan Hollow Fiber DialyzersFJI · Traditional | Idemsa | 04/17/2000SE |
| K992594 | A-15 HemodialyzerFJI · Traditional | Althin Medical AB | 09/24/1999SE |
| K992565 | A-18 HemodialyzerFJI · Traditional | Althin Medical AB | 09/23/1999SE |
| K991512 | Asahi Am-R-Series Dialyzers (Modified), Model Am-Nr-XFJI · Traditional | Asahi Medical Co., Ltd. | 07/29/1999SE |
More from Asahi Medical Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K955299 | DPS 4 Dialyzer Preparation SystemLIF · Traditional | 10/21/1996SE |
| K931336 | DRS 4 Dialyzer Reprocessing SystemLIF · Traditional | 04/18/1996SE |
| K944539 | DRS 4 ND Dialyzer Reprocessing SystemLIF · Traditional | 11/29/1995SE |
| K923529 | DMS Data Management SYSTEM/DRS-4 Dialyzer ReprocesLIF · Traditional | 08/29/1994SE |
| K914580 | DRS-4 Dialyzer Reprocessing SystemLIF · Traditional | 02/24/1992SE |
| K874573 | Fresenius Puristeril 340 (TM)LIF · Traditional | 04/25/1988SE |
| K874872 | Fresenius Hemoflow F3, F4, F5, F7FJI · Traditional | 02/19/1988SE |
| K870724 | Fresenius Hemoflow F60 and F80KDI · Traditional | 04/01/1987SE |
| K864587 | Fresenius Ultraflux AV400, AV600KDI · Traditional | 03/03/1987SE |
| K864169 | Fresenius Hemoflow F50 & F70KDI · Traditional | 11/06/1986SE |
Questions and answers
When was Fresenius Hemoflow F6 and F8 cleared by the FDA?
Fresenius Hemoflow F6 and F8 (K870725) received a 510(k) decision of Substantially Equivalent on May 1, 1987, 66 days after the submission was received.
What is the product code of K870725?
The FDA product code is FJI – Dialyzer, Capillary, Hollow Fiber, a Class II (moderate risk) device regulated under 21 CFR 876.5820.