FDA 510(k) Application Details - K041781

Device Classification Name	Compressor, Air, Portable   More FDA Info for this Device
510(K) Number	K041781
Device Name	Compressor, Air, Portable
Applicant	HAMILTON MEDICAL AG PO BOX 30008 RENO, NV 89502 US Other 510(k) Applications for this Company
Contact	J. DAVID THOMPSON Other 510(k) Applications for this Contact
Regulation Number	868.6250   More FDA Info for this Regulation Number
Classification Product Code	BTI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/01/2004
Decision Date	03/14/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review