VISITEC VITRECTOMY UNIT— 510(k) K896622
Substantially EquivalentVisitec Co.
FDA 510(k) clearance K896622 for VISITEC VITRECTOMY UNIT, Substantially Equivalent on 1990-04-04. Applicant: Visitec Co.. Device class: 2.
Clearance details
- Applicant
- Visitec Co.
- Product code
- Code HKP
- Device class
- Class 2
- Regulation
- 21 CFR 886.4150
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Sarasota, FL, US
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