510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K153731Substantially Equivalent

LifeFlow Rapid Infusion Device (LifeFlow Device)

410 Medical Innovation, LLC, Durham NC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K153731 is the FDA 510(k) clearance record for LifeFlow Rapid Infusion Device (LifeFlow Device), a class II device, cleared for 410 Medical Innovation, LLC on under FDA product code FPA (Set, Administration, Intravascular). FDA records list one 510(k) clearance for 410 Medical Innovation, LLC. As of , FDA records show no recalls naming K153731.

Clearance record

Decision date
Received
(241 days to decision)
Product code
FPA Set, Administration, Intravascular
Regulation
21 CFR 880.5440
Device class
Class II
Review panel
General Hospital
Applicant
410 Medical Innovation, LLC 201 W. Main St., Suite 305, Durham NC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FPA

Trailing 12 months
5 clearances under product code FPA in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FPA, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20260
April 20260
May 20261
June 20261
July 20260
August 20260
September 20261
October 20260