FDA 510(k)

AlphaVac MMA F1885 System (H787253020)

K-Number: K240397 · 2024-04-01

Decision Date2024-04-01

Product CodeQEZ

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

AlphaVac MMA F1885 System (H787253020) is the device name listed in this FDA 510(k) record. The listed applicant is AngioDynamics, Inc.. It received FDA 510(k) clearance on 2024-04-01 under 510(k) 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. The listed applicant is AngioDynamics, Inc.. The 510(k) number is K240397.

When did AlphaVac MMA F1885 System (H787253020) receive FDA 510(k) clearance?

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

Who is the listed applicant for AlphaVac MMA F1885 System (H787253020)?

The FDA 510(k) record lists AngioDynamics, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

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Related Devices (Code: QEZ)

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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.