FDA 510(k) K163524, Vessel Dilator, by Fetzer Medical GmbH & Co. KG
FDA 510(k) K163524, Vessel Dilator, by Fetzer Medical GmbH & Co. KG
FDA 510(k) records for Vessel Dilator (K163524), submitted by Fetzer Medical GmbH.
- 510(k) Number: K163524
- Applicant: Fetzer Medical GmbH
- Decision Date: 06/29/2017
- Decision: Substantially Equivalent (SESE)
- Product Code: DWP DWP
- Review Panel: Cardiovascular
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