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FDA 510(k)

Mojo 2 Full Face Vented Mask; Veraseal 3 Full Face Vented Mask; V3 Full Face Vented Mask

K-Number: K241661 · 2024-07-10

Decision Date2024-07-10
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Mojo 2 Full Face Vented Mask; Veraseal 3 Full Face Vented Mask; V3 Full Face Vented Mask is a medical device manufactured by Sleepnet Corporation. It received FDA 510(k) clearance on 2024-07-10 under approval number K241661. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Mojo 2 Full Face Vented Mask; Veraseal 3 Full Face Vented Mask; V3 Full Face Vented Mask?

Mojo 2 Full Face Vented Mask; Veraseal 3 Full Face Vented Mask; V3 Full Face Vented Mask is a medical device that received FDA 510(k) clearance on 2024-07-10. It is manufactured by Sleepnet Corporation. The 510(k) number is K241661.

When was Mojo 2 Full Face Vented Mask; Veraseal 3 Full Face Vented Mask; V3 Full Face Vented Mask approved by the FDA?

Mojo 2 Full Face Vented Mask; Veraseal 3 Full Face Vented Mask; V3 Full Face Vented Mask received FDA 510(k) clearance on 2024-07-10, under approval number K241661.

What company makes Mojo 2 Full Face Vented Mask; Veraseal 3 Full Face Vented Mask; V3 Full Face Vented Mask?

Mojo 2 Full Face Vented Mask; Veraseal 3 Full Face Vented Mask; V3 Full Face Vented Mask is manufactured by Sleepnet Corporation.

What is the FDA product code for Mojo 2 Full Face Vented Mask; Veraseal 3 Full Face Vented Mask; V3 Full Face Vented Mask?

The FDA product code for Mojo 2 Full Face Vented Mask; Veraseal 3 Full Face Vented Mask; V3 Full Face Vented Mask is BZD.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.