510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K032276Substantially Equivalent

Click Holter

Remco Italia S.p.A., South Pedrino Di Vignate, Mi., IT / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K032276 is the FDA 510(k) clearance record for CLICK HOLTER, a class II device, cleared for Remco Italia S.P.A. on under FDA product code MWJ (Electrocardiograph, Ambulatory (Without Analysis)). FDA records list 3 510(k) clearances for Remco Italia S.P.A., from to . As of , FDA records show no recalls naming K032276.

Clearance record

Decision date
Received
(35 days to decision)
Product code
MWJ Electrocardiograph, Ambulatory (Without Analysis)
Regulation
21 CFR 870.2800
Device class
Class II
Review panel
Cardiovascular
Applicant
Remco Italia S.P.A. Via Rivoltana Nuova 53, South Pedrino Di Vignate, Mi., IT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MWJ

Trailing 12 months
5 clearances under product code MWJ in the twelve months to October 2026, June 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code MWJ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20262
July 20260
August 20261
September 20262
October 20260