FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

ES-Series

K Number: K260748 · Decision Jun 9, 2026
Classifications
1
FEI Numbers
220
Registration Numbers
220
Same Product Code
1171
Applicant Total
4
Review Days
95

Basic Information

Device Name
ES-Series
K Number
K260748
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1550
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
E-Scopics
Date Received
March 6, 2026
Decision Date
June 9, 2026
Product Code
IYN
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
IYN System, Imaging, Pulsed Doppler, Ultrasonic

Similar 510(k) Clearances

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

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Other Clearances by E-Scopics

K Number Device Name
K260589 ES-Series
K232336 ES Series V2
K213102 ES1 System