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
6
Applicant Total
10
Review Days
140

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

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
K252844 Tyto Insights for Wheeze Detection (with PCCP)
DEN250014 Tyto Insights for Eardrum Bulging Detection
K252089 Tyto Stethoscope (G3)
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