510(k) K234002

Device
ICEfx Cryoablation System (FPRCH8000-02)
Applicant
Boston Scientific
510(k) number
K234002
Product code
GEH
Decision
Substantially Equivalent (SESE)
Decision date
2024-03-13
Date received
2023-12-19
Regulation
878.4350
Classification name
Unit, Cryosurgical, Accessories
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Benjamin Van Santen
Address
1 Scimed Pl. Maple Grove MN US 55311 55311

FDA Registration Numbers

Source Documents

510(k) summary PDF

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