510(k) K172049
K172049 is an FDA 510(k) premarket notification submitted by Cry IQ AB for the device "CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED". The FDA issued a decision of Substantially Equivalent on Aug 30, 2017. The device falls under product code GEH (Unit, Cryosurgical, Accessories), a Class II device regulated under 21 CFR 878.4350.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 30, 2017
- Date Received
- Jul 6, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Unit, Cryosurgical, Accessories
- Device Class
- Class II
- Regulation Number
- 878.4350
- Review Panel
- SU
- Submission Type
- 510(k)