FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

Tyto Insights for Rhonchi Detection

K Number: K243567 · Decision Apr 7, 2025
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
5
Applicant Total
7
Review Days
140

Basic Information

Device Name
Tyto Insights for Rhonchi Detection
K Number
K243567
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1900
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tyto Care Ltd.
Date Received
November 18, 2024
Decision Date
April 7, 2025
Product Code
PHZ
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PHZ Abnormal Breath Sound Device

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PHZ), ordered by most recent decision date.

View all

Other Clearances by Tyto Care Ltd.

K Number Device Name
K240555 Tyto Insights for Crackles Detection
K232237 Tyto Insights for Wheeze Detection
K221614 TytoCare Lung Sounds Analyzer
K190242 Tyto Thermometer
K181612 Tyto Stethoscope (OTC)
K160401 Tyto Stethoscope