510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K884800Substantially Equivalent

Acta Genos Electrocardiograph

Parexel Intl. Corp., Cambridge MS / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K884800 is the FDA 510(k) clearance record for ACTA GENOS ELECTROCARDIOGRAPH, a class II device, cleared for Parexel Intl. Corp. on under FDA product code DPS (Electrocardiograph). FDA records list 14 510(k) clearances for Parexel Intl. Corp., from to . As of , FDA records show no recalls naming K884800.

Clearance record

Decision date
Received
(218 days to decision)
Product code
DPS Electrocardiograph
Regulation
21 CFR 870.2340
Device class
Class II
Review panel
Cardiovascular
Applicant
Parexel Intl. Corp. One Alewife Pl., Cambridge MS
Third party review
No

Clearances, product code DPS

Trailing 12 months
5 clearances under product code DPS in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DPS, trailing twelve months
MonthClearances
November 20251
December 20251
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20261
October 20260