TrueFit Bolus; TrueFlex Bolus— 510(k) K243057

Substantially Equivalent

Adaptiiv Medical Technologies, Inc.

FDA 510(k) clearance K243057 for TrueFit Bolus; TrueFlex Bolus, Substantially Equivalent on 2024-10-23. Applicant: Adaptiiv Medical Technologies, Inc..

Clearance details

Applicant: Adaptiiv Medical Technologies, Inc.
Product code: Code MUJ
Advisory panel: Radiology
Date received: 2024-09-27
Decision date: 2024-10-23
Decision: Substantially Equivalent
Clearance type: Special
Location: Halifax, CA

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