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FDA 510(k)

AlphaVac MMA F1885 System (H787253020)

K-Number: K240397 · 2024-04-01

ApplicantAngioDynamics, Inc.
Decision Date2024-04-01
Product CodeQEZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AlphaVac MMA F1885 System (H787253020) is a medical device manufactured by AngioDynamics, Inc.. It received FDA 510(k) clearance on 2024-04-01 under approval number K240397. The device is classified under product code QEZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AlphaVac MMA F1885 System (H787253020)?

AlphaVac MMA F1885 System (H787253020) is a medical device that received FDA 510(k) clearance on 2024-04-01. It is manufactured by AngioDynamics, Inc.. The 510(k) number is K240397.

When was AlphaVac MMA F1885 System (H787253020) approved by the FDA?

AlphaVac MMA F1885 System (H787253020) received FDA 510(k) clearance on 2024-04-01, under approval number K240397.

What company makes AlphaVac MMA F1885 System (H787253020)?

AlphaVac MMA F1885 System (H787253020) is manufactured by AngioDynamics, Inc..

What is the FDA product code for AlphaVac MMA F1885 System (H787253020)?

The FDA product code for AlphaVac MMA F1885 System (H787253020) is QEZ.

Related Clinical Trials

NCT07280247 Acute Pulmonary Embolism Treatment With the AlphaVac Multipurpose Mechanical Aspiration System and the AlphaReturn Blood Management System: Evaluation of Safety and Effectiveness RECRUITING NCT06453876 Percutaneous Embolectomy, Low Dose Thrombolysis or Heparin for Intermediate High Risk Pulmonary Embolism (STRATIFY II) NOT_YET_RECRUITING

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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.

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