# Thayer Medical Corp.

- Location (FDA's records): Tucson, AZ
- FDA decisions: 19 (1988–2024): 19 510(k) clearances
- Names in FDA's records: Thayer Medical Corp. (15); Thayer Medical Corporation (4)
- Product codes: CAF (9), BYH (4), NVP (2), CAI (1), BZA (1), BXR (1), BZO (1)
- Predicates its devices cite: 4 (4 its own); citations of its devices by later devices: 4 (4 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K102658: Minispacer Dual-Spray Mdi Adapter with 22MM (or 15MM) OD / 22MM OD/ID Connections  / 15MM ID Connections (2010), cited by 1
- K111570: Minispacer (R) Mdi Adapter with Counter Incrementing Actuator (2011), cited by 1
- K160109: Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber (2017), cited by 1
- K993101: Liteaire (2000), cited by 1

## Recent decisions
- K233553: MiniSpacer® 1024, 1025, 1543 and 1024A, 1025A, 1543A Dual Spray MDI Adapter (Jun 18, 2024)
- K210558: LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber (Apr 1, 2022)
- K160109: Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber (May 19, 2017)
- K111570: Minispacer (R) Mdi Adapter with Counter Incrementing Actuator (Sep 29, 2011)
- K102658: Minispacer Dual-Spray Mdi Adapter with 22MM (or 15MM) OD / 22MM OD/ID Connections  / 15MM ID Connections (Dec 10, 2010)
- K993101: Liteaire (Oct 26, 2000)
- K992722: Primeaire (Nov 10, 1999)
- K972237: Hand Held Medispacer (Jul 31, 1997)

Source page: https://510kreport.com/company/thayer-medical