TUTOPLAST DURA— 510(k) K910555
Substantially EquivalentPfrimmer-Viggo GmbH & Co.
FDA 510(k) clearance K910555 for TUTOPLAST DURA, Substantially Equivalent on 1992-04-20. Applicant: Pfrimmer-Viggo GmbH & Co.. Device class: 2.
Clearance details
- Applicant
- Pfrimmer-Viggo GmbH & Co.
- Product code
- Code LEM
- Device class
- Class 2
- Regulation
- 21 CFR 882.5975
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Recent devices under product code LEM
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