510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K040802Substantially Equivalent

Hemosonic 200Hemodynamic Monitor

Arrow Intl., Inc., Reading PA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K040802 is the FDA 510(k) clearance record for HEMOSONIC 200HEMODYNAMIC MONITOR, a class II device, cleared for Arrow Intl., Inc. on under FDA product code DPN (Thin Layer Chromatography, Propoxyphene). FDA records list 111 510(k) clearances for Arrow Intl., Inc., from to . As of , FDA records show no recalls naming K040802.

Clearance record

Decision date
Received
(30 days to decision)
Product code
DPN Thin Layer Chromatography, Propoxyphene
Regulation
21 CFR 862.3700
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Arrow Intl., Inc. 2400 Bernville Rd., Reading PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DPN

Trailing 12 months

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

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