Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Premarket Approval (PMA)
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceLungFit PH
Generic NameNitric Oxide Generator and Delivery System
ApplicantBeyond Air, Inc.
825 E. Gate Blvd., Suite 320
Garden City, NY 11530
PMA NumberP200044
Supplement NumberS003
Date Received05/01/2023
Decision Date09/10/2023
Product Code QTB 
Advisory Committee Anesthesiology
Supplement TypeReal-Time Process
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
Approval for minor software changes to add support for future language translations, enhance manfucaturability and serviceability, refine alarms, limit the range for date changes, and for preparation of future compatibility and enhancements.
-
-