510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K000500Substantially Equivalent

Dinamap Advanced Nibp Module

Critikon Company, LLC, Tampa FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K000500 is the FDA 510(k) clearance record for DINAMAP ADVANCED NIBP MODULE, a class II device, cleared for Critikon Company, LLC on under FDA product code DXN (System, Measurement, Blood-Pressure, Non-Invasive). FDA records list 51 510(k) clearances for Critikon Company, LLC, from to . As of , FDA records show no recalls naming K000500.

Clearance record

Decision date
Received
(102 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
Critikon Company, LLC 4502 Woodland Corporate Blvd., Tampa FL
510(k) summary
Summary
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