Vessel Dilator— 510(k) K163524
Substantially EquivalentFetzer Medical GmbH & Co. KG
FDA 510(k) clearance K163524 for Vessel Dilator, Substantially Equivalent on 2017-06-29. Applicant: Fetzer Medical GmbH & Co. KG. Device class: 2.
Clearance details
- Applicant
- Fetzer Medical GmbH & Co. KG
- Product code
- Code DWP
- Device class
- Class 2
- Regulation
- 21 CFR 870.4475
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tuttlingen, DE
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More clearances from Fetzer Medical GmbH & Co. KG
view allData sourced from openFDA. This site is unofficial and independent of the FDA.