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)

mediCAD Web

K-Number: K183412 · 2019-10-31

ApplicantMedicad Hectec GmbH
Decision Date2019-10-31
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

mediCAD Web is a medical device manufactured by Medicad Hectec GmbH. It received FDA 510(k) clearance on 2019-10-31 under approval number K183412. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the mediCAD Web?

mediCAD Web is a medical device that received FDA 510(k) clearance on 2019-10-31. It is manufactured by Medicad Hectec GmbH. The 510(k) number is K183412.

When was mediCAD Web approved by the FDA?

mediCAD Web received FDA 510(k) clearance on 2019-10-31, under approval number K183412.

What company makes mediCAD Web?

mediCAD Web is manufactured by Medicad Hectec GmbH.

What is the FDA product code for mediCAD Web?

The FDA product code for mediCAD Web is LLZ.

Other Devices by Medicad Hectec GmbH

K170702mediCAD 4.0

Related Devices (Code: LLZ)

K161959ClearView cCADClearview Diagnostics, Inc. K163539Ez3D-i / E3Ewoosoft Co., Ltd. K162955Multi-Modality Tumor Tracking (MMTT) applicationPhilips Medical Systems Nederland B.V. K160852ZiaZetta Medical Technologies, LLC K162376CAAS MR 4D FlowPie Medical Imaging BV K161322CT CoPilotZepmed, LLC

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.

↑