Atlas FDA

Inessa System

FDA 510(k) clearance K230545 · decided 2023-12-20

Clearance details

K-number
K230545
Device name
Inessa System
Applicant
Triple Jump Israel , Ltd.
Decision
Substantially Equivalent
Date received
2023-02-28
Decision date
2023-12-20
Days to decision
295 days
Clearance type
Traditional
Product code
QFG
Device class
2
Regulation number
880.5730
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Yokneam Lllit, IL
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.