510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K024019Substantially Equivalent

Arterialflow System, Model 32A

Aircast, Inc., Summit NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K024019 is the FDA 510(k) clearance record for ARTERIALFLOW SYSTEM, MODEL 32A, a class II device, cleared for Aircast, Inc. on under FDA product code JOW (Sleeve, Limb, Compressible). FDA records list 11 510(k) clearances for Aircast, Inc., from to . As of , FDA records show no recalls naming K024019.

Clearance record

Decision date
Received
(180 days to decision)
Product code
JOW Sleeve, Limb, Compressible
Regulation
21 CFR 870.5800
Device class
Class II
Review panel
Cardiovascular
Applicant
Aircast, Inc. 92 River Rd., Summit NJ
510(k) summary
Statement
Third party review
No

Clearances, product code JOW

Trailing 12 months
8 clearances under product code JOW in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code JOW, trailing twelve months
MonthClearances
November 20250
December 20252
January 20260
February 20261
March 20260
April 20261
May 20260
June 20261
July 20261
August 20261
September 20261
October 20260