SPECTRALIS Software V.7.2-US
by Heidelberg Engineering GmbH
SPECTRALIS Software V.7.2-US is a Class II device made by Heidelberg Engineering GmbH, cleared under FDA 510(k) K241163 on 11 Oct 2024 (1 earlier submission) and listed in FDA GUDID since 4 Oct 2024 (UDI-DI 04059237001027), active as of 12 Nov 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK241163 | Date11 Oct 2024 | StatusActive |
| United States | GUDID listing | Number04059237001027 | Date4 Oct 2024 | StatusListed |
Official records
- AccessGUDID record 04059237001027
- FDA 510(k) database K241163
- FDA 510(k) database K240221
Across registries
- FDA 510(k) K241163 decided 11 Oct 2024 Active
- FDA GUDID UDI-DI 04059237001027 listed 4 Oct 2024 Listed
Timeline
- Cleared FDA 510(k) K240221
- Listed FDA GUDID 04059237001027
- Cleared FDA 510(k) K241163
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Spectralis
- Generic name
- Scanning-laser retinal imaging system
- Model / reference
- Software V.7.2-US
- Primary DI / UDI-DI
- 04059237001027
- FDA product code
- MYC, OBO
- GMDN term
- Scanning-laser retinal imaging system
- Device class
- Class II
- Regulation number
- 886.1570
- GUDID distribution status
- In Commercial Distribution
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