AIMAGO EASYLDI MICROCIRCULATION CAMERA
FDA 510(k) clearance K121429 · decided 2012-08-10
Clearance details
- K-number
- K121429
- Device name
- AIMAGO EASYLDI MICROCIRCULATION CAMERA
- Applicant
- Aimago SA
- Decision
- Substantially Equivalent
- Date received
- 2012-05-14
- Decision date
- 2012-08-10
- Days to decision
- 88 days
- Clearance type
- Traditional
- Product code
- DPT
- Device class
- 2
- Regulation number
- 870.2120
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Lausanne, CH
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.