MEDI-6000 MEDICAL IMAGE DIGITIZER— 510(k) K091288
Substantially EquivalentMicrotek International, Inc.
FDA 510(k) clearance K091288 for MEDI-6000 MEDICAL IMAGE DIGITIZER, Substantially Equivalent on 2009-08-14. Applicant: Microtek International, Inc.. Device class: 2.
Clearance details
- Applicant
- Microtek International, Inc.
- 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
- Guisan, Taoyuan, TW
Recent devices under product code LMA
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