510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K021240Substantially Equivalent

Eikon Automatic Digital Blood Pressure Monitor, Model Hd-200M/hd-200

Eikon Healthcare Device Corp., Hsin-Chu City,, TW / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K021240 is the FDA 510(k) clearance record for EIKON AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-200M/HD-200, a class II device, cleared for Eikon Healthcare Device Corp. on under FDA product code DXN (System, Measurement, Blood-Pressure, Non-Invasive). FDA records list 2 510(k) clearances for Eikon Healthcare Device Corp. As of , FDA records show no recalls naming K021240.

Clearance record

Decision date
Received
(204 days to decision)
Product code
DXN System, Measurement, Blood-Pressure, Non-Invasive
Regulation
21 CFR 870.1130
Device class
Class II
Review panel
Cardiovascular
Applicant
Eikon Healthcare Device Corp. No 58, Fu-Chiun St., Hsin-Chu City,, TW
510(k) summary
Statement
Third party review
No

Clearances, product code DXN

Trailing 12 months
30 clearances under product code DXN in the twelve months to October 2026, April 2026 the highest month at 5.
Show the numbers
Monthly 510(k) clearances under FDA product code DXN, trailing twelve months
MonthClearances
November 20250
December 20251
January 20262
February 20264
March 20262
April 20265
May 20263
June 20264
July 20262
August 20264
September 20262
October 20261