RTLX— 510(k) K992392
Substantially EquivalentInfimed, Inc.
FDA 510(k) clearance K992392 for RTLX, Substantially Equivalent on 2000-03-31. Applicant: Infimed, Inc.. Device class: 2.
Clearance details
- Applicant
- Infimed, Inc.
- Product code
- Code MUH
- Device class
- Class 2
- Regulation
- 21 CFR 872.1800
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Liverpool, NY, US
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