CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED
K-Number: K172049 · 2017-08-30
Device Summary
Frequently Asked Questions
What is the CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED?
CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED is a medical device that received FDA 510(k) clearance on 2017-08-30. The listed applicant is Cry IQ AB. The 510(k) number is K172049.
When did CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED receive FDA 510(k) clearance?
CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED received FDA 510(k) clearance on 2017-08-30, under 510(k) number K172049.
Who is the listed applicant for CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED?
The FDA 510(k) record lists Cry IQ AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED?
The FDA product code for CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED is GEH.
Related Devices (Code: GEH)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.