510(k) K223163

Device
Sleepiz One+
Applicant
Sleepiz AG
510(k) number
K223163
Product code
DRT
Decision
Substantially Equivalent (SESE)
Decision date
2023-08-18
Date received
2022-10-07
Regulation
870.2300
Classification name
Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
Yes

Related Records

Applicant Contact

Contact
Marta Stepien
Address
Hornbachstrasse 23 Zurich CH 8008 8008

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
07649996477019Sleepiz One+Sleepiz AG2024-05-14

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