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)

InVivo Web Viewer

K-Number: K181926 · 2018-09-21

ApplicantAnatomage, Inc.
Decision Date2018-09-21
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

InVivo Web Viewer is a medical device manufactured by Anatomage, Inc.. It received FDA 510(k) clearance on 2018-09-21 under approval number K181926. 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 InVivo Web Viewer?

InVivo Web Viewer is a medical device that received FDA 510(k) clearance on 2018-09-21. It is manufactured by Anatomage, Inc.. The 510(k) number is K181926.

When was InVivo Web Viewer approved by the FDA?

InVivo Web Viewer received FDA 510(k) clearance on 2018-09-21, under approval number K181926.

What company makes InVivo Web Viewer?

InVivo Web Viewer is manufactured by Anatomage, Inc..

What is the FDA product code for InVivo Web Viewer?

The FDA product code for InVivo Web Viewer is LLZ.

Other Devices by Anatomage, Inc.

K161270CephSimulation

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.

↑