Capillary Flow Dialyzers Models ST-12 & ST-15

FDA 510(k) K871471 · Travenol Laboratories, S.A.

Substantially Equivalent

510(k) numberK871471

Submission

Device name
Capillary Flow Dialyzers Models ST-12 & ST-15
Applicant
Travenol Laboratories, S.A.
Round Lake, IL, US
Received
April 14, 1987
Decision date
June 12, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

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

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K002761Fresnius Hemoflow F7NR, F50NR, F70NR HemodialyzersFJI · Traditional Fresenius Medical Care North America12/04/2000SE
K991908Idemsa Hemophan Hollow Fiber DialyzersFJI · Traditional Idemsa04/17/2000SE
K992594A-15 HemodialyzerFJI · Traditional Althin Medical AB09/24/1999SE
K992565A-18 HemodialyzerFJI · Traditional Althin Medical AB09/23/1999SE
K991512Asahi Am-R-Series Dialyzers (Modified), Model Am-Nr-XFJI · Traditional Asahi Medical Co., Ltd.07/29/1999SE

More from Asahi Medical Co., Ltd.

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K874181Baxter Bedside SystemFRN · Traditional 02/22/1988SE
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K873873Resubmitted Micron Transfusion FilterCAK · Traditional 10/22/1987SE
K873984Automatic Peritoneal Dialysis Cycler Set (5C4437)KDJ · Traditional 10/20/1987SE
K872364Hemodialysis (SPS), Model 550, Code 5M1309FII · Traditional 10/13/1987SE
K872652Upgraded Auto Peritoneal Dialysis Cycler SystemFKX · Traditional 09/30/1987SE
K870801Flo-Gard 6200 Volumetric Infusion/Pumping BloodFRN · Traditional 09/04/1987SE
K871908IV Administration SetBRZ · Traditional 07/27/1987SE
K865029Continu-Flo Solution Admin. Set W/In-Line FilterFPB · Traditional 04/17/1987SE
K870169Capillary Flow DialyzersFJI · Traditional 04/06/1987SE

Questions and answers

When was Capillary Flow Dialyzers Models ST-12 & ST-15 cleared by the FDA?

Capillary Flow Dialyzers Models ST-12 & ST-15 (K871471) received a 510(k) decision of Substantially Equivalent on June 12, 1987, 59 days after the submission was received.

What is the product code of K871471?

The FDA product code is FJI – Dialyzer, Capillary, Hollow Fiber, a Class II (moderate risk) device regulated under 21 CFR 876.5820.