VES 1501-M— 510(k) K982409
Substantially EquivalentAngiolaz, Inc.
FDA 510(k) clearance K982409 for VES 1501-M, Substantially Equivalent on 1998-08-21. Applicant: Angiolaz, Inc.. Device class: 1.
Clearance details
- Applicant
- Angiolaz, Inc.
- Product code
- Code FWF
- Device class
- Class 1
- Regulation
- 21 CFR 878.4160
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bellows Falls, VT, US
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More clearances from Angiolaz, Inc.
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