K-number	K213717
Device name	AIR Recon DL
Applicant	Ge Medical Systems,Llc (Ge Healthcare)
Product code	LNH
Device class	Class II
Decision date	Jun 8, 2022
Decision	Substantially Equivalent
Regulation	892.1000

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Source

View the full FDA submission: accessdata.fda.gov

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AIR Recon DL

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