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FDA 510(k) K240782 CellFX Percutaneous Electrode System Full Submission
FDA 510(k) K240782 CellFX Percutaneous Electrode System Full Submission
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Original Request: I am requesting the full FDA 510(k) documents for K240782 Pulse Biosciences CellFX Percutaneous Electrode System (Product Code GEI) Cleared 8/5/24.
Tags: MedTech, 510(k), 2024
Tags: MedTech, 510(k), 2024
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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