FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Swoop Portable MR Imaging System

K Number: K223247 · Decision Dec 6, 2022
Classifications
1
FEI Numbers
152
Registration Numbers
152
Same Product Code
1071
Applicant Total
12
Review Days
46

Basic Information

Device Name
Swoop Portable MR Imaging System
K Number
K223247
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hyperfine, Inc.
Date Received
October 21, 2022
Decision Date
December 6, 2022
Product Code
LNH
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LNH System, Nuclear Magnetic Resonance Imaging

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Other Clearances by Hyperfine, Inc.

K Number Device Name
K250236 Swoop® Portable MR Imaging® System (V2)
K251276 Swoop® Portable MR Imaging® System
K240944 Swoop® Portable MR Imaging® System
K232760 Swoop® Portable MR Imaging System®
K230208 Swoop® Portable MR Imaging System™
K223268 BrainInsight
K221923 Swoop Portable MR Imaging System
K220815 BrainInsight
K221393 Swoop Portable MR Imaging System
K212456 Swoop Point-of-Care Magnetic Resonance Imaging (POC MRI) Scanner System
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