FDA 510(k) Application Details - K992214

Device Classification Name	Calculator, Pulmonary Function Data   More FDA Info for this Device
510(K) Number	K992214
Device Name	Calculator, Pulmonary Function Data
Applicant	ERICH JAEGER B.V. REGULIERENING 11 NL-3981 LA BUNNIK NL-3981 NL Other 510(k) Applications for this Company
Contact	LEO DEN BAKKER 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	07/01/1999
Decision Date	02/22/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review