Disposable Dialyzers, Sd-Id, SD-2D

FDA 510(k) K790308 · Bentley Laboratories, Inc.

Substantially Equivalent

510(k) numberK790308

Submission

Device name
Disposable Dialyzers, Sd-Id, SD-2D
Applicant
Bentley Laboratories, Inc.
Mchenry, IL, US
Received
February 13, 1979
Decision date
May 1, 1979
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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K010366Disposable Storage CapFJI · Abbreviated Molded Products, Inc.11/28/2001SE
K011148Ultraconcentrator SystemFJI · Special Interpore Cross Intl.06/13/2001SE
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

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Questions and answers

When was Disposable Dialyzers, Sd-Id, SD-2D cleared by the FDA?

Disposable Dialyzers, Sd-Id, SD-2D (K790308) received a 510(k) decision of Substantially Equivalent on May 1, 1979, 77 days after the submission was received.

What is the product code of K790308?

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