Blood Port Cap, Luer-Lock Fitting, Dayspring Medical Part No. BPC252LL

FDA 510(k) K961026 · Dayspring Medical, Inc.

Substantially Equivalent

510(k) numberK961026

Submission

Device name
Blood Port Cap, Luer-Lock Fitting, Dayspring Medical Part No. BPC252LL
Applicant
Dayspring Medical, Inc.
Boulder, CO, US
Received
March 14, 1996
Decision date
June 10, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

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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More from Asahi Medical Co., Ltd.

510(k)DeviceDecision
K991005Vented Diakysate Port Ccap, Red Pliable Vinyl - Dayspring Medical Part No, DPC101VSLLB · Traditional 06/22/1999SE
K991003Pump Segment Rinse Line W/ Slip-On Connector, Pump Segment Rinse Line W/ Luer-Lock…FKY · Traditional 06/09/1999SE
K961039Bllod Port Cap, Dialysate Port Cap, Vented Dialysate Port Cap with Red Pliable VinylFJI · Traditional 09/12/1996SE
K961040Blood Port Cap, Dialysate Port Cap, Red Hard PlasticFJI · Traditional 06/11/1996SE

Questions and answers

When was Blood Port Cap, Luer-Lock Fitting, Dayspring Medical Part No. BPC252LL cleared by the FDA?

Blood Port Cap, Luer-Lock Fitting, Dayspring Medical Part No. BPC252LL (K961026) received a 510(k) decision of Substantially Equivalent on June 10, 1996, 88 days after the submission was received.

What is the product code of K961026?

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