BVI SLING— 510(k) K002233
Substantially EquivalentBio-Vascular, Inc.
FDA 510(k) clearance K002233 for BVI SLING, Substantially Equivalent on 2000-10-13. Applicant: Bio-Vascular, Inc.. Device class: 2.
Clearance details
- Applicant
- Bio-Vascular, Inc.
- Product code
- Code PAJ
- Device class
- Class 2
- Regulation
- 21 CFR 878.3300
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Paul, MN, US
Recent devices under product code PAJ
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Data sourced from openFDA. This site is unofficial and independent of the FDA.