FDA 510(k) Application Details - K001502

Device Classification Name	Calculator, Pulmonary Function Data   More FDA Info for this Device
510(K) Number	K001502
Device Name	Calculator, Pulmonary Function Data
Applicant	ERICH JAEGER GMBH 22705 SAVI RANCH PKWY. YORBA LINDA, CA 92887-4645 US Other 510(k) Applications for this Company
Contact	LARRY MURDOCK Other 510(k) Applications for this Contact
Regulation Number	868.1880   More FDA Info for this Regulation Number
Classification Product Code	BZC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/15/2000
Decision Date	07/12/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review