510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K913595Substantially Equivalent

Ds-240 Ambulatory Blood Pressure Monitoring System

Koven and Assoc., Inc., St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913595 is the FDA 510(k) clearance record for DS-240 AMBULATORY BLOOD PRESSURE MONITORING SYSTEM, a class II device, cleared for Koven and Assoc., Inc. on under FDA product code DXN (System, Measurement, Blood-Pressure, Non-Invasive). FDA records list 8 510(k) clearances for Koven and Assoc., Inc., from to . As of , FDA records show no recalls naming K913595.

Clearance record

Decision date
Received
(227 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
Koven and Assoc., Inc. The Trade Center, St. Louis MO
510(k) summary
Statement
Third party review
No

Clearances, product code DXN

Trailing 12 months
29 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 20260