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

SubtleMR (2.3.x)

K Number: K223623 · Decision May 11, 2023
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
11
Review Days
157

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Basic Information

Device Name
SubtleMR (2.3.x)
K Number
K223623
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Subtle Medical, Inc.
Date Received
December 5, 2022
Decision Date
May 11, 2023
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

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Other Clearances by Subtle Medical, Inc.

K Number Device Name
K254120 SubtleHD-CT (1.x)
K254013 SubtleHD-PET (1.x)
K243250 SubtleHD (1.x)
K240290 AiMIFY (1.x)
K241329 SubtleSYNTH (1.x)
K233699 SubtleREFORMAT (1.x)
K211964 SubtlePET
K203182 SubtleMR
K191688 SubtleMR
K182336 SubtlePET
Search all 11 clearances from Subtle Medical, Inc. →