Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Claritag Advanced

K-Number: K222356 · 2023-05-18

ApplicantDgi Technologies
Decision Date2023-05-18
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Claritag Advanced is the device name listed in this FDA 510(k) record. The listed applicant is Dgi Technologies. It received FDA 510(k) clearance on 2023-05-18 under 510(k) number K222356. 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 Claritag Advanced?

Claritag Advanced is a medical device that received FDA 510(k) clearance on 2023-05-18. The listed applicant is Dgi Technologies. The 510(k) number is K222356.

When did Claritag Advanced receive FDA 510(k) clearance?

Claritag Advanced received FDA 510(k) clearance on 2023-05-18, under 510(k) number K222356.

Who is the listed applicant for Claritag Advanced?

The FDA 510(k) record lists Dgi Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Claritag Advanced?

The FDA product code for Claritag Advanced is GEH.

Other records listing Dgi Technologies as applicant

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.

K190747Claritag

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.

K261068Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000)Serpex MedicalK261806ERBECRYO 2 Cryosurgical Unit and AccessoriesErbe Elektromedizin GmbHK253230ERBECRYO 2 Cryosurgical Unit and Accessories: ERBECRYO 2 cryosurgical unit; Erbe Flexible CryoprobeErbe Elektromedizin GmbHK252198Advanced Cryo Skin Tag Remover (Advanced Skin Tag Remover)Medical Brands Laboratories B.V.K260377XSense Cryoablation System with CryoProbesIceCure Medical , Ltd.K251928CoolCryo - Cryoapplicator for cardiac cryoablation (CC01-01); CoolCryo - Control console for cardiac cryoablation with liquid nitrogen reservoir (CC01-21)Medinice S.A.

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.

↑