MiniSpacer® 1024, 1025, 1543 and 1024A, 1025A, 1543A Dual Spray MDI Adapter

FDA 510(k) K233553 · Thayer Medical Corporation

Substantially Equivalent

510(k) numberK233553

Submission

Device name
MiniSpacer® 1024, 1025, 1543 and 1024A, 1025A, 1543A Dual Spray MDI Adapter
Applicant
Thayer Medical Corporation
Tucson, AZ, US
Received
November 6, 2023
Decision date
June 18, 2024
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CAF – Nebulizer (Direct Patient Interface)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5630
Specialty
Anesthesiology

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Questions and answers

When was MiniSpacer® 1024, 1025, 1543 and 1024A, 1025A, 1543A Dual Spray MDI Adapter cleared by the FDA?

MiniSpacer® 1024, 1025, 1543 and 1024A, 1025A, 1543A Dual Spray MDI Adapter (K233553) received a 510(k) decision of Substantially Equivalent on June 18, 2024, 225 days after the submission was received.

What is the product code of K233553?

The FDA product code is CAF – Nebulizer (Direct Patient Interface), a Class II (moderate risk) device regulated under 21 CFR 868.5630.