LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM— 510(k) K052797
Substantially EquivalentMedtek Devices, Inc.
FDA 510(k) clearance K052797 for LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM, Substantially Equivalent on 2006-02-13. Applicant: Medtek Devices, Inc.. Device class: 2.
Clearance details
- Applicant
- Medtek Devices, Inc.
- Product code
- Code FYD
- Device class
- Class 2
- Regulation
- 21 CFR 878.5070
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Buffalo, NY, US
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