FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Focused Cryotherapy System

K Number: K250742 · Decision Dec 9, 2025
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
261
Applicant Total
1
Review Days
273

Basic Information

Device Name
Focused Cryotherapy System
K Number
K250742
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4350
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Focused Cryo, Inc.
Date Received
March 11, 2025
Decision Date
December 9, 2025
Product Code
GEH
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
GEH Unit, Cryosurgical, Accessories

Similar 510(k) Clearances

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

View all