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FDA Device Info: Zeller Power Products 510k Info
FDA Device Info: Zeller Power Products 510k Info
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Records pertaining to Zeller Power Products, Battery Beast, or Douglas R. Austin regarding 510(K) or FDA actions regarding violations related to the manufacture and sale of AED batteries. [REQ YEAR: 2022]
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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