FDA 510(k) Application Details - K242374

Device Classification Name	Apparatus, Nitric Oxide Delivery   More FDA Info for this Device
510(K) Number	K242374
Device Name	Apparatus, Nitric Oxide Delivery
Applicant	Airgas Therapeutics LLC 6141 Easton Rd. P.O. Box 310 Plumsteadville, PA 18949 US Other 510(k) Applications for this Company
Contact	Timothy Warren Other 510(k) Applications for this Contact
Regulation Number	868.5165   More FDA Info for this Regulation Number
Classification Product Code	MRN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/09/2024
Decision Date	01/17/2025
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