Atlas FDA

SnapshotNIR

FDA 510(k) clearance K201976 · decided 2020-11-10

Clearance details

K-number
K201976
Device name
SnapshotNIR
Applicant
Kent Imaging
Decision
Substantially Equivalent
Date received
2020-07-16
Decision date
2020-11-10
Days to decision
117 days
Clearance type
Traditional
Product code
MUD
Device class
2
Regulation number
870.2700
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Calgary, CA
Third-party review
No
Expedited review
No

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Devices cleared under the same product code - the starting set for predicate research.

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SnapshotNIR model KD205 (K240601)Kent Imaging, Inc.2024-04-02
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Intra.Ox™ 2.0 Handheld Tissue Oximeter (K233488)Vioptix, Inc.2024-02-28
Edwards Algorithm for Measurement of Blood Hemoglobin (K230612)Edwards Lifesciences, LLC2023-11-17
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Recalls involving this device

RecordFirmDate
Snapshot NIR, REF: KD204 recall (Z-0789-2024)KENT IMAGING, INC.2024-01-25