FDA 510(k) clearance · back to tracker

Swoop® Portable MR Imaging® System

Hyperfine, Inc. cleared K253489 on 2025-12-12, decision: substantially equivalent

K-number

K253489

Sponsor

Hyperfine, Inc.

Device

Swoop® Portable MR Imaging® System

Class

Class II

Decision

Substantially Equivalent

Decision date

2025-12-12

Product code

LNH

Advisory committee

Radiology

Medical specialty

Radiology

Regulation number

892.1000

Official FDA record

Open K253489on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

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Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.