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510(k) K122247

LIDCORAPID V2 MONITOR by Lidco, Ltd. — Product Code DXG

K122247 is an FDA 510(k) premarket notification submitted by Lidco, Ltd. for the device "LIDCORAPID V2 MONITOR". The FDA issued a decision of Substantially Equivalent on March 20, 2013. The device falls under product code DXG (Computer, Diagnostic, Pre-Programmed, Single-Function), a Class II device regulated under 21 CFR 870.1435. Lidco, Ltd. has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 20, 2013
Date Received
July 27, 2012
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Computer, Diagnostic, Pre-Programmed, Single-Function
Device Class
Class II
Regulation Number
870.1435
Review Panel
CV
Submission Type

Other clearances by Lidco, Ltd.

  • K163334 — LiDCOunity v2 Hemodynamic Monitor (June 5, 2017)
  • K152935 — LiDCOunity Monitor (March 17, 2016)
  • K131048 — LIDCO CNAP MODULE (August 28, 2013)
  • K023960 — LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70 (January 9, 2003)
  • K010049 — PULSECO HEMODYNAMIC MONITOR CM71 (June 14, 2001)
  • K962918 — LIDCO SYSTEM (January 8, 1999)

Other clearances for product code DXG

  • K253092 — Argos Infinity (Rev. 1.0) (February 13, 2026)
  • K251275 — VitalStream ART Connect; VitalStream-Hemo (September 26, 2025)
  • K232048 — Cogent™ Hemodynamic Monitoring System; Cogent™ HMS (December 20, 2023)
  • K212529 — Hypotension Decision Assist Model HDA-OR2 (November 23, 2021)
  • K192169 — PulsioFlex Monitoring System with ProAQT Sensor (April 30, 2020)
  • K193179 — EV1000 Clinical Platform (December 17, 2019)
  • K190955 — Hypotension Decision Assist (November 27, 2019)
  • K181372 — Argos (December 13, 2018)
  • K172259 — PulsioFlex Monitoring System (January 18, 2018)
  • K163334 — LiDCOunity v2 Hemodynamic Monitor (June 5, 2017)

FDA data resources