InstaRISPACS / InstaZFP / InstaMobi v5.0— 510(k) K182572

Name: FDA 510(k) clearance K182572
Creator: U.S. Food and Drug Administration
Published: 2019-04-12

Substantially Equivalent

Meddiff Technologies Pvt. , Ltd.

FDA 510(k) clearance K182572 for InstaRISPACS / InstaZFP / InstaMobi v5.0, Substantially Equivalent on 2019-04-12. Applicant: Meddiff Technologies Pvt. , Ltd.. Device class: 2.

Clearance details

Applicant: Meddiff Technologies Pvt. , Ltd.
Product code: Code LLZ
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2018-09-18
Decision date: 2019-04-12
Decision: Substantially Equivalent
Clearance type: Special
Location: Bangalore, IN

Download summary PDF View on FDA.gov ↗

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K120718 — INSTAPACS/INSTARISPACS2012-04-19

Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.