FDA 510(k) Application Details - K961468

Device Classification Name	Vaporizer, Anesthesia, Non-Heated   More FDA Info for this Device
510(K) Number	K961468
Device Name	Vaporizer, Anesthesia, Non-Heated
Applicant	PENLON LTD. ABINGDON OXFORDSHIRE OX14 3PH GB Other 510(k) Applications for this Company
Contact	ALAN C GREEN Other 510(k) Applications for this Contact
Regulation Number	868.5880   More FDA Info for this Regulation Number
Classification Product Code	CAD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/17/1996
Decision Date	07/16/1996
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