INFRASCANNER, MODEL 1000— 510(k) DEN100002
UnknownInfrascan, Inc.
FDA 510(k) clearance DEN100002 for INFRASCANNER, MODEL 1000, Unknown on 2011-12-13. Applicant: Infrascan, Inc.. Device class: 2.
Clearance details
- Applicant
- Infrascan, Inc.
- Product code
- Code OPT
- Device class
- Class 2
- Regulation
- 21 CFR 882.1935
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- Philadelphia, PA, US
Recent devices under product code OPT
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