LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber
K-Number: K210558 · 2022-04-01
Device Summary
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. The listed applicant is Thayer Medical Corporation. The 510(k) number is K210558.
When did LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber receive FDA 510(k) clearance?
LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber received FDA 510(k) clearance on 2022-04-01, under 510(k) number K210558.
Who is the listed applicant for LiteAire Basic 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 LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber?
The FDA product code for LiteAire Basic 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.