510(k) K211818

Swoop Point-of-Care Magnetic Resonance Imaging (POC MRI) Scanner System by Hyperfine, Inc. — Product Code LNH

K211818 is an FDA 510(k) premarket notification submitted by Hyperfine, Inc. for the device "Swoop Point-of-Care Magnetic Resonance Imaging (POC MRI) Scanner System". The FDA issued a decision of Substantially Equivalent on July 7, 2021. The device falls under product code LNH (System, Nuclear Magnetic Resonance Imaging), a Class II device regulated under 21 CFR 892.1000. Hyperfine, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 7, 2021
Date Received
June 11, 2021
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Nuclear Magnetic Resonance Imaging
Device Class
Class II
Regulation Number
892.1000
Review Panel
RA
Submission Type