FDA 510(k) Application Details - K041974

Device Classification Name	Compressor, Air, Portable   More FDA Info for this Device
510(K) Number	K041974
Device Name	Compressor, Air, Portable
Applicant	MED2000 S.R.L. 55 NORTHERN BLVD., STE 200 GREAT NECK, NY 11021 US Other 510(k) Applications for this Company
Contact	SUSAN D GOLDSTEIN-FALK 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	07/22/2004
Decision Date	08/24/2004
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