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FDA 510(k)

LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber

K-Number: K210558 · 2022-04-01

Decision Date2022-04-01
Product CodeNVP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber is a medical device manufactured by Thayer Medical Corporation. It received FDA 510(k) clearance on 2022-04-01 under approval number K210558. The device is classified under product code NVP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber?

LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber is a medical device that received FDA 510(k) clearance on 2022-04-01. It is manufactured by Thayer Medical Corporation. The 510(k) number is K210558.

When was LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber approved by the FDA?

LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber received FDA 510(k) clearance on 2022-04-01, under approval number K210558.

What company makes LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber?

LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber is manufactured by Thayer Medical Corporation.

What is the FDA product code for LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber?

The FDA product code for LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber is NVP.

Other Devices by Thayer Medical Corporation

Related Devices (Code: NVP)

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.