510(k) K171398
K171398 is an FDA 510(k) premarket notification submitted by R2 Dermatology ,Inc for the device "Dermal Cooling System". The FDA issued a decision of Substantially Equivalent on Jul 6, 2017. The device falls under product code GEH (Unit, Cryosurgical, Accessories), a Class II device regulated under 21 CFR 878.4350. R2 Dermatology ,Inc has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jul 6, 2017
- Date Received
- May 12, 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)