510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K122247Substantially Equivalent

Lidcorapid V2 Monitor

Lidco Ltd, London, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K122247 is the FDA 510(k) clearance record for LIDCORAPID V2 MONITOR, a class II device, cleared for Lidco, Ltd. on under FDA product code DXG (Computer, Diagnostic, Pre-Programmed, Single-Function). FDA records list 6 510(k) clearances for Lidco, Ltd., from to . As of , FDA records show no recalls naming K122247.

Clearance record

Decision date
Received
(236 days to decision)
Product code
DXG Computer, Diagnostic, Pre-Programmed, Single-Function
Regulation
21 CFR 870.1435
Device class
Class II
Review panel
Cardiovascular
Applicant
Lidco, Ltd. 16 Orsman Rd., London, GB
510(k) summary
Statement
Third party review
No

Clearances, product code DXG

Trailing 12 months
1 clearance under product code DXG in the twelve months to October 2026, February 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DXG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260