510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K232035Substantially Equivalent

Impala

AliveCor, Mountain View CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K232035 is the FDA 510(k) clearance record for Impala, a class II device, cleared for AliveCor, Inc. on under FDA product code DPS (Electrocardiograph). FDA records list 19 510(k) clearances for AliveCor, Inc., from to . As of , FDA records show no recalls naming K232035.

Clearance record

Decision date
Received
(336 days to decision)
Product code
DPS Electrocardiograph
Regulation
21 CFR 870.2340
Device class
Class II
Review panel
Cardiovascular
Applicant
AliveCor, Inc. 189 N. Bernardo Ave., Mountain View CA
510(k) summary
Summary PDF
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