P200MAAF
FDA 510(k) clearance K102492 · decided 2010-09-30
Clearance details
- K-number
- K102492
- Device name
- P200MAAF
- Applicant
- Optos Plc.
- Decision
- Substantially Equivalent
- Date received
- 2010-08-31
- Decision date
- 2010-09-30
- Days to decision
- 30 days
- Clearance type
- Special
- Product code
- MYC
- Device class
- 2
- Regulation number
- 886.1570
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Washington, DC, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| OcuMet Beacon (OCUB100) (K241931) | Ocusciences, Inc. | 2025-04-22 |
| MAIA (AHMACME001) (K243504) | Centervue S.P.A. | 2025-03-17 |
| DRSplus (K213705) | Centervue S.P.A. | 2021-12-21 |
| EIDON FA, EIDON, EIDON AF, EIDON UWFL (K211328) | Centervue S.P.A. | 2021-08-19 |
| DRSplus (K192113) | Centervue S.P.A. | 2019-11-15 |
| EIDON FA (K180526) | Centervue S.P.A. | 2018-07-16 |
| Retia 2 (K180293) | Centervue S.P.A. | 2018-05-30 |
| MAIA (K153181) | Centervue S.P.A. | 2016-06-08 |
| COMPASS (K150320) | Centervue S.P.A. | 2015-06-30 |
| P200DTx (K142897) | Optos Plc. | 2015-01-16 |
| EIDON (K142047) | Centervue S.P.A. | 2014-11-12 |
| DAYTONA ICG (P200TICG) (K134039) | Optos Plc. | 2014-04-11 |
Recalls involving this device
No recalls on record reference this clearance.