Dynavisc— 510(k) K262343
Substantially EquivalentFziomed, Inc.
FDA 510(k) clearance K262343 for Dynavisc, Substantially Equivalent on 2026-10-28. Applicant: Fziomed, Inc.. Device class: 2.
Clearance details
- Applicant
- Fziomed, Inc.
- Product code
- Product code OWW
- 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
- San Luis Obispo, CA, US
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