510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K132026Substantially Equivalent

V Series Monitoring System, 12.1 Dcu/v12 and 21.0 Dcu/v21

Datascope Corp., Mahwh NJ / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K132026 is the FDA 510(k) clearance record for V SERIES MONITORING SYSTEM, 12.1 DCU/V12 AND 21.0 DCU/V21, a class II device, cleared for Mindray DS USA, Inc. on under FDA product code MHX (Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)). FDA records list 139 510(k) clearances for Datascope Corp., from to . As of , FDA records show one recall naming K132026.

Clearance record

Decision date
Received
(172 days to decision)
Product code
MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Regulation
21 CFR 870.1025
Device class
Class II
Review panel
Cardiovascular
Applicant
Mindray DS USA, Inc. 800 Macarthur Blvd., Mahwh NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MHX

Trailing 12 months
15 clearances under product code MHX in the twelve months to October 2026, April 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code MHX, trailing twelve months
MonthClearances
November 20251
December 20251
January 20261
February 20261
March 20260
April 20263
May 20262
June 20261
July 20261
August 20263
September 20261
October 20260