# K973291: Dynamic Hollow Fiber Dialyzer DC-Series

- Pathway: 510(k) (Traditional)
- Applicant: Dynamic Technology Corp.
- Decided: Dec 19, 1997 after 108 days
- Product code: FJI (Dialyzer, Capillary, Hollow Fiber)
- Device class: 2
- Regulation: 21 CFR 876.5820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K864831 (1987). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K864831: Cobe Centrysystem 145E,160E,175E,190E Dialyzers, Cobe Laboratories, Inc. (1987) Summary page 1.
- (no number) Baxter CF25: named in the summary without a submission number
- (no number) Terumo Clirans T175: named in the summary without a submission number
- (no number) Terumo Clirans T174: named in the summary without a submission number

## Most influential descendants
- K990159: Dynamic Hollow Fiber Dialyzer DH-Series, Model AH 90111 (1999), 0 descendants of its own
- K982134: Dynamic Hollow Fiber Dialyzer DS-Series Model as-851 (1999), 0 descendants of its own

## Indications for use
The DYNAMIC Hollow Fiber Dialyzer DC-Series are indicated for use whenever a patient is in acute or chronic renal failure and hemodialysis is prescribed by a physician. Therefore, use of this device should be only on the direction of a physician who has evaluated all of the aspects of the patient's illness.

Source page: https://510kreport.com/device/K973291
Methodology: https://510kreport.com/methodology