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

FDA 510(k)

C-Lant Port

K-Number: K252714 · 2026-02-27

ApplicantVigor Medical Technologies , Ltd.
Decision Date2026-02-27
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

C-Lant Port is a medical device manufactured by Vigor Medical Technologies , Ltd.. It received FDA 510(k) clearance on 2026-02-27 under approval number K252714. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C-Lant Port?

C-Lant Port is a medical device that received FDA 510(k) clearance on 2026-02-27. It is manufactured by Vigor Medical Technologies , Ltd.. The 510(k) number is K252714.

When was C-Lant Port approved by the FDA?

C-Lant Port received FDA 510(k) clearance on 2026-02-27, under approval number K252714.

What company makes C-Lant Port?

C-Lant Port is manufactured by Vigor Medical Technologies , Ltd..

What is the FDA product code for C-Lant Port?

The FDA product code for C-Lant Port is GCJ.

Related Devices (Code: GCJ)

K163102ReliaCatch Specimen Retrieval Bag 10mm; ReliaCatch Specimen Retrieval Bag 12mmCovidien K160801Well Lead Extraction BagWell Lead Medical Co., Ltd. K153773Disposal Lens Cleaning SheathOlympus Medical Systems Corp. K161720Standard ClampStandard Bariatrics K162445LiVac Retractor SystemLivac Pty, Ltd. K162584VersaOne Bladeless TrocarCovidien

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.

↑