MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE— 510(k) K061404
Substantially EquivalentFci Ophthalmics, Inc.
FDA 510(k) clearance K061404 for MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE, Substantially Equivalent on 2006-08-07. Applicant: Fci Ophthalmics, Inc.. Device class: Unclassified.
Clearance details
- Applicant
- Fci Ophthalmics, Inc.
- Product code
- Code OKS
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Centercille, MA, US
Recent devices under product code OKS
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