FDA 510(k)

InstaRISPACS / InstaZFP / InstaMobi v5.0

K-Number: K182572 · 2019-04-12

ApplicantMeddiff Technologies Pvt. , Ltd.

Decision Date2019-04-12

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

InstaRISPACS / InstaZFP / InstaMobi v5.0 is a medical device manufactured by Meddiff Technologies Pvt. , Ltd.. It received FDA 510(k) clearance on 2019-04-12 under approval number K182572. 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 InstaRISPACS / InstaZFP / InstaMobi v5.0?

InstaRISPACS / InstaZFP / InstaMobi v5.0 is a medical device that received FDA 510(k) clearance on 2019-04-12. It is manufactured by Meddiff Technologies Pvt. , Ltd.. The 510(k) number is K182572.

When was InstaRISPACS / InstaZFP / InstaMobi v5.0 approved by the FDA?

InstaRISPACS / InstaZFP / InstaMobi v5.0 received FDA 510(k) clearance on 2019-04-12, under approval number K182572.

What company makes InstaRISPACS / InstaZFP / InstaMobi v5.0?

InstaRISPACS / InstaZFP / InstaMobi v5.0 is manufactured by Meddiff Technologies Pvt. , Ltd..

What is the FDA product code for InstaRISPACS / InstaZFP / InstaMobi v5.0?

The FDA product code for InstaRISPACS / InstaZFP / InstaMobi v5.0 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.