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)

DG PACS

K-Number: K152977 · 2016-01-25

ApplicantDicom Grid, Inc.
Decision Date2016-01-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DG PACS is a medical device manufactured by Dicom Grid, Inc.. It received FDA 510(k) clearance on 2016-01-25 under approval number K152977. 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 DG PACS?

DG PACS is a medical device that received FDA 510(k) clearance on 2016-01-25. It is manufactured by Dicom Grid, Inc.. The 510(k) number is K152977.

When was DG PACS approved by the FDA?

DG PACS received FDA 510(k) clearance on 2016-01-25, under approval number K152977.

What company makes DG PACS?

DG PACS is manufactured by Dicom Grid, Inc..

What is the FDA product code for DG PACS?

The FDA product code for DG PACS is LLZ.

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.

↑