FDA 510(k) Application Details - K051313

Device Classification Name	Ventilatory Effort Recorder   More FDA Info for this Device
510(K) Number	K051313
Device Name	Ventilatory Effort Recorder
Applicant	SALTER LABS 100 W. SYCAMORE RD. ARVIN, CA 93203 US Other 510(k) Applications for this Company
Contact	DUANE KAZAL Other 510(k) Applications for this Contact
Regulation Number	868.2375   More FDA Info for this Regulation Number
Classification Product Code	MNR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/19/2005
Decision Date	09/15/2005
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