510(k) K252043

Device
Bipolar applicator CelonProBreath (WB990310); Bipolar applicator CelonProSleep plus (WB990311); Bipolar applicator CelonProBreath (WB990210); Bipolar applicator CelonProSleep plus (WB990211)
Applicant
Olympus Winter & Ibe GmbH
510(k) number
K252043
Product code
GEI
Decision
Substantially Equivalent (SESE)
Decision date
2025-09-23
Date received
2025-06-30
Regulation
878.4400
Classification name
Electrosurgical, Cutting & Coagulation & Accessories
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Michaela Soukopova
Address
Kuehnstrasse 61 Hamburg DE 22045 22045

FDA Registration Numbers

Source Documents

510(k) summary PDF

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