FDA 510(k) Application Details - K140559

Device Classification Name	Chamber, Hyperbaric   More FDA Info for this Device
510(K) Number	K140559
Device Name	Chamber, Hyperbaric
Applicant	SECHRIST INDUSTRIES, INC. 4225 EAST LA PALMA AVE. ANAHEIM, CA 92807 US Other 510(k) Applications for this Company
Contact	VICTOR C ARELLANO Other 510(k) Applications for this Contact
Regulation Number	868.5470   More FDA Info for this Regulation Number
Classification Product Code	CBF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/05/2014
Decision Date	05/30/2014
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review