510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K243236Substantially Equivalent

WHOOP ECG (electrocardiogram) Feature (1.0)

Whoop, Inc., Boston MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K243236 is the FDA 510(k) clearance record for WHOOP ECG (electrocardiogram) Feature (1.0), a class II device, cleared for Whoop., Inc. on under FDA product code QDA (Electrocardiograph Software For Over-The-Counter Use). FDA's definition for product code QDA reads: "An electrocardiograph software device for over-the-counter use creates, analyzes, and displays electrocardiograph data, and can provide information for identifying cardiac arrhythmias. This device is not intended to provide a diagnosis". FDA records list one 510(k) clearance for Whoop., Inc. As of , FDA records show no recalls naming K243236.

Clearance record

Decision date
Received
(176 days to decision)
Product code
QDA Electrocardiograph Software For Over-The-Counter Use
Regulation
21 CFR 870.2345
Device class
Class II
Review panel
Cardiovascular
Applicant
Whoop., Inc. One Kenmore Sq., Boston MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code QDA

Trailing 12 months

FDA records hold no clearances under product code QDA in the trailing twelve months.

FDA records show no clearances under product code QDA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code QDA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260