MP-1 MICRO PERIMETER
FDA 510(k) clearance K023719 · decided 2002-12-23
Clearance details
- K-number
- K023719
- Device name
- MP-1 MICRO PERIMETER
- Applicant
- Nidek Technologies Srl
- Decision
- Substantially Equivalent
- Date received
- 2002-11-05
- Decision date
- 2002-12-23
- Days to decision
- 48 days
- Clearance type
- Traditional
- Product code
- HKI
- Device class
- 2
- Regulation number
- 886.1120
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Vigonza (Padova), IT
- Third-party review
- Yes
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.