510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K251812Substantially Equivalent

Steripath® Flow™ Blood Collection System

Magnolia Medical Technologies, Inc., Seattle WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K251812 is the FDA 510(k) clearance record for Steripath® Flow™ Blood Collection System, a class II device, cleared for Magnolia Medical Technologies on under FDA product code JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection). FDA records list 4 510(k) clearances for Magnolia Medical Technologies, from to . As of , FDA records show no recalls naming K251812.

Clearance record

Decision date
Received
(105 days to decision)
Product code
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
Regulation
21 CFR 862.1675
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Magnolia Medical Technologies 220 W Mercer St., Seattle WA
510(k) summary
Statement
Third party review
No

Clearances, product code JKA

Trailing 12 months
6 clearances under product code JKA in the twelve months to October 2026, April 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code JKA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20263
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260