Bunnell Inc 436 Lawndale Dr Salt Lake City Ut 84115 Pma Numberp850064 Supplement Numbers047 Date Received03 07 2022 Decision Date03 31 2022 Product Code Lsz Advisory Committee Anesthesiology Supplement Type30 Day Notice Supplement Reason Process Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No

FDA Filings

This page includes the latest FDA filings for Bunnell Inc 436 Lawndale Dr Salt Lake City Ut 84115 Pma Numberp850064 Supplement Numbers047 Date Received03 07 2022 Decision Date03 31 2022 Product Code Lsz Advisory Committee Anesthesiology Supplement Type30 Day Notice Supplement Reason Process Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

FDA Filings

Device
Company
DeviceDate
BUNNELL, INC.436 Lawndale Dr.salt Lake City, UT 84115 PMA NumberP850064 Supplement NumberS047 Date Received03/07/2022 Decision Date03/31/2022 Product Code LSZ  Advisory Committee Anesthesiology Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
LifePulse High Frequency Ventilator2022-03-31

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