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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 the device name listed in this FDA 510(k) record. The listed applicant is Thayer Medical Corporation. It received FDA 510(k) clearance on 2017-05-19 under 510(k) 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. The listed applicant is Thayer Medical Corporation. The 510(k) number is K160109.

When did Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber receive FDA 510(k) clearance?

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

Who is the listed applicant for Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber?

The FDA 510(k) record lists Thayer Medical Corporation as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Thayer Medical Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: NVP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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