FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

MOVIVA® Hybrid Ablation Probe

K Number: K253915 · Decision Dec 18, 2025
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
16
Review Days
10

Basic Information

Device Name
MOVIVA® Hybrid Ablation Probe
K Number
K253915
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Erbe Elektromedizin GmbH
Date Received
December 8, 2025
Decision Date
December 18, 2025
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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