Class Class II
CLARUS (700) (K243878)
Description
CLARUS (700) by Carl Zeiss Meditec, Inc., an FDA 510(k) cleared ophthalmic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK243878
Clearance Date2025-04-17
Clearance TypeTraditional
Product CodeQER
Regulation Number886.1120
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243878
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. CLARUS (700) (K243878) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K191194 | CLARUS | Carl Zeiss Meditec, Inc. | 2019 |
Trace the full predicate network for K243878
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.