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FDA 510(k)

CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED

K-Number: K172049 · 2017-08-30

ApplicantCry IQ AB
Decision Date2017-08-30
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED is a medical device manufactured by Cry IQ AB. It received FDA 510(k) clearance on 2017-08-30 under approval number K172049. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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. It is manufactured by Cry IQ AB. The 510(k) number is K172049.

When was CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED approved by the FDA?

CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED received FDA 510(k) clearance on 2017-08-30, under approval number K172049.

What company makes CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED?

CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED is manufactured by Cry IQ AB.

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.

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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.

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