FDA 510(k) Application Details - K962924

Device Classification Name	Meter, Peak Flow, Spirometry   More FDA Info for this Device
510(K) Number	K962924
Device Name	Meter, Peak Flow, Spirometry
Applicant	HEALTHSCAN PRODUCTS, INC. 908 POMPTON AVE. UNIT B2 CEDAR GROVE, NJ 07009-1292 US Other 510(k) Applications for this Company
Contact	LAUREN R ZIEGLER Other 510(k) Applications for this Contact
Regulation Number	868.1860   More FDA Info for this Regulation Number
Classification Product Code	BZH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/29/1996
Decision Date	10/25/1996
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