VISIJET HYDROKERATOME, MODEL 50— 510(k) K991124
Substantially EquivalentVisijet, Inc.
FDA 510(k) clearance K991124 for VISIJET HYDROKERATOME, MODEL 50, Substantially Equivalent on 2000-10-20. Applicant: Visijet, Inc.. Device class: 1.
Clearance details
- Applicant
- Visijet, Inc.
- Product code
- Code MYD
- Device class
- Class 1
- Regulation
- 21 CFR 886.4370
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.