FDA 510(k) Application Details - K102658

Device Classification Name	Nebulizer (Direct Patient Interface)   More FDA Info for this Device
510(K) Number	K102658
Device Name	Nebulizer (Direct Patient Interface)
Applicant	THAYER MEDICAL CORP. 4575 SOUTH PALO VERDE RD., SUITE 337 TUCSON, AZ 85714-1961 US Other 510(k) Applications for this Company
Contact	JAMES M STRICKLAND Other 510(k) Applications for this Contact
Regulation Number	868.5630   More FDA Info for this Regulation Number
Classification Product Code	CAF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/15/2010
Decision Date	12/10/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review