510(k) K233553

Device
MiniSpacer® 1024, 1025, 1543 and 1024A, 1025A, 1543A Dual Spray MDI Adapter
Applicant
Thayer Medical Corporation
510(k) number
K233553
Product code
CAF
Decision
Substantially Equivalent (SESE)
Decision date
2024-06-18
Date received
2023-11-06
Regulation
868.5630
Classification name
Nebulizer (Direct Patient Interface)
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
James Strickland
Address
4575 S Palo Verde Rd., Suite 337 Tucson AZ US 85714 85714

FDA Registration Numbers

Source Documents

510(k) summary PDF

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