FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇹 Italy
COMPASS
K Number: K150320
·
Decision Jun 30, 2015
Classifications
1
FEI Numbers
12
Registration Numbers
13
Same Product Code
21
Applicant Total
7
Review Days
141
Basic Information
- Device Name
- COMPASS
- K Number
- K150320
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 886.1570
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- CENTERVUE SPA
- Date Received
- February 9, 2015
- Decision Date
- June 30, 2015
- Product Code
- MYC
- Advisory Committee
- Ophthalmic
- Review Advisory Committee
- OP
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MYC | Ophthalmoscope, Laser, Scanning | FDA class 2 | Ophthalmic |
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Other Clearances by CENTERVUE SPA
| K Number | Device Name | ||
|---|---|---|---|
| K243504 | MAIA (AHMACME001) | Mar 17, 2025 | Substantially Equivalent |
| K153181 | MAIA | Jun 8, 2016 | Substantially Equivalent |
| K142047 | EIDON | Nov 12, 2014 | Substantially Equivalent |
| K133758 | CENTERVUE MACULAR INTEGRITY ASSESSMENT | Apr 23, 2014 | Substantially Equivalent |
| K101935 | CENTERVUE DIGITAL RETINOGRAPHY SYSTEM | Oct 27, 2010 | Substantially Equivalent |
| K092187 | MAIA, MODEL 1 | May 27, 2010 | Substantially Equivalent |