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

Tyto Stethoscope (G3)

K Number: K252089 · Decision Mar 12, 2026
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
153
Applicant Total
10
Review Days
253

Basic Information

Device Name
Tyto Stethoscope (G3)
K Number
K252089
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1875
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tyto Care , Ltd.
Date Received
July 2, 2025
Decision Date
March 12, 2026
Product Code
DQD
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DQD Stethoscope, Electronic

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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
K243567 Tyto Insights for Rhonchi Detection
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