KONICA KFDR-S— 510(k) K896739
Substantially EquivalentKonica Medical Corp.
FDA 510(k) clearance K896739 for KONICA KFDR-S, Substantially Equivalent on 1990-04-30. Applicant: Konica Medical Corp.. Device class: 2.
Clearance details
- Applicant
- Konica Medical Corp.
- Product code
- Code LMA
- Device class
- Class 2
- Regulation
- 21 CFR 892.2030
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
Recent devices under product code LMA
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