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
K254240Substantially Equivalent

Echo-2

Neko Health AB, Danderyd, SE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

Clearance record

Decision date
Received
(267 days to decision)
Product code
QOK Hardware And Software For Optical Camera-Based Measurement Of Heart Rate And Respiratory Rate
Regulation
21 CFR 870.2786
Device class
Class II
Review panel
Cardiovascular
Applicant
Neko Health AB Svärdvägen 19, Danderyd, SE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code QOK

Trailing 12 months
1 clearance under product code QOK in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code QOK, 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 20261
October 20260