510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K961040Substantially Equivalent

Blood Port Cap, Dialysate Port Cap, Red Hard Plastic

Dayspring Medical, Inc., Boulder CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K961040 is the FDA 510(k) clearance record for BLOOD PORT CAP, DIALYSATE PORT CAP, RED HARD PLASTIC, a class II device, cleared for Dayspring Medical, Inc. on under FDA product code FJI (Dialyzer, Capillary, Hollow Fiber). FDA records list 5 510(k) clearances for Dayspring Medical, Inc., from to . As of , FDA records show no recalls naming K961040.

Clearance record

Decision date
Received
(89 days to decision)
Product code
FJI Dialyzer, Capillary, Hollow Fiber
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Dayspring Medical, Inc. 1936 Beacon Ct., Boulder CO
510(k) summary
Statement
Third party review
No

Clearances, product code FJI

Trailing 12 months

FDA records hold no clearances under product code FJI in the trailing twelve months.

FDA records show no clearances under product code FJI in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FJI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260