ZEPTO Precision Capsulotomy System— 510(k) K221188
Substantially EquivalentCentricity Vision, Inc.
FDA 510(k) clearance K221188 for ZEPTO Precision Capsulotomy System, Substantially Equivalent on 2022-06-23. Applicant: Centricity Vision, Inc.. Device class: 2.
Clearance details
- Applicant
- Centricity Vision, Inc.
- Product code
- Code PUL
- Device class
- Class 2
- Regulation
- 21 CFR 886.4100
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Carlsbad, CA, US
Recent devices under product code PUL
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