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FDA 510(k)

Freeze Point & Private Label Versions

K-Number: K242625 · 2024-10-25

ApplicantCryoconcepts LP
Decision Date2024-10-25
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Freeze Point & Private Label Versions is a medical device manufactured by Cryoconcepts LP. It received FDA 510(k) clearance on 2024-10-25 under approval number K242625. 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 Freeze Point & Private Label Versions?

Freeze Point & Private Label Versions is a medical device that received FDA 510(k) clearance on 2024-10-25. It is manufactured by Cryoconcepts LP. The 510(k) number is K242625.

When was Freeze Point & Private Label Versions approved by the FDA?

Freeze Point & Private Label Versions received FDA 510(k) clearance on 2024-10-25, under approval number K242625.

What company makes Freeze Point & Private Label Versions?

Freeze Point & Private Label Versions is manufactured by Cryoconcepts LP.

What is the FDA product code for Freeze Point & Private Label Versions?

The FDA product code for Freeze Point & Private Label Versions is GEH.

Related Clinical Trials

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Related PubMed Literature

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Related Devices (Code: 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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