510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K884390Substantially Equivalent

Intersept* Crystalloid Cardioplegia Filter

Medtronic Blood Systems, Inc., Anaheim CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K884390 is the FDA 510(k) clearance record for INTERSEPT* CRYSTALLOID CARDIOPLEGIA FILTER, a class II device, cleared for Medtronic Blood Systems, Inc. on under FDA product code KRJ (Filter, Prebypass, Cardiopulmonary Bypass). FDA records list 15 510(k) clearances for Medtronic Blood Systems, Inc., from to . As of , FDA records show no recalls naming K884390.

Clearance record

Decision date
Received
(64 days to decision)
Product code
KRJ Filter, Prebypass, Cardiopulmonary Bypass
Regulation
21 CFR 870.4280
Device class
Class II
Review panel
Cardiovascular
Applicant
Medtronic Blood Systems, Inc. 4633 E. Lapalma Ave., Anaheim CA
Third party review
No

Clearances, product code KRJ

Trailing 12 months

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

FDA records show no clearances under product code KRJ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KRJ, 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