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FDA 510(k)

Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber

K-Number: K160109 · 2017-05-19

Decision Date2017-05-19
Product CodeNVP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber is a medical device manufactured by Thayer Medical Corporation. It received FDA 510(k) clearance on 2017-05-19 under approval number K160109. 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 Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber?

Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber is a medical device that received FDA 510(k) clearance on 2017-05-19. It is manufactured by Thayer Medical Corporation. The 510(k) number is K160109.

When was Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber approved by the FDA?

Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber received FDA 510(k) clearance on 2017-05-19, under approval number K160109.

What company makes Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber?

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

What is the FDA product code for Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber?

The FDA product code for Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber is NVP.

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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.