510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K920778Substantially Equivalent

Omron Wrist Digital Blood Pressure Monitor Hem-601

Omron Healthcare Co., Ltd., Vernon Hills IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K920778 is the FDA 510(k) clearance record for OMRON WRIST DIGITAL BLOOD PRESSURE MONITOR HEM-601, a class II device, cleared for Omron Healthcare, Inc. on under FDA product code DXN (System, Measurement, Blood-Pressure, Non-Invasive). FDA records list 68 510(k) clearances for Omron Healthcare, Inc., from to . As of , FDA records show no recalls naming K920778.

Clearance record

Decision date
Received
(308 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
Omron Healthcare, Inc. 300 Lakeview Pkwy., Vernon Hills IL
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 November 2026, April 2026 the highest month at 5.
Show the numbers
Monthly 510(k) clearances under FDA product code DXN, trailing twelve months
MonthClearances
December 20251
January 20262
February 20264
March 20262
April 20265
May 20263
June 20264
July 20262
August 20264
September 20262
October 20261
November 20260