IOLAB LACRIMAL DUCT CATHETER— 510(k) K935233
Substantially EquivalentChiron Vision Corp.
FDA 510(k) clearance K935233 for IOLAB LACRIMAL DUCT CATHETER, Substantially Equivalent on 1994-09-15. Applicant: Chiron Vision Corp.. Device class: Unclassified.
Clearance details
- Applicant
- Chiron Vision Corp.
- Product code
- Code OKS
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
Recent devices under product code OKS
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