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FDA PowerFlow IV Port (K191143) Full Document Request
FDA PowerFlow IV Port (K191143) Full Document Request
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Original Request: The disclosable portions of any and all documents and records concerning the PowerFlowTM Implantable Apheresis IV Port (K191143), including but not limited to memoranda, reports, summaries, briefing documents, presentations, slide decks, reviews, analyses, meeting minutes, notes, letters, emails, facsimiles, telephone logs, etc., from January 1, 2017 to present.
Tags: MedTech, 510(k), 2017
Tags: MedTech, 510(k), 2017
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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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