510(k) K242801

Device
MICOR 700 System (N/A); MICOR 700 drive (FG-50631); MICOR 700 extractor (FG-50621); MICOR 700 vitrector (FG-51185)
Applicant
Carl Zeiss Meditec Cataract Technology, Inc.
510(k) number
K242801
Product code
HQC
Decision
Substantially Equivalent (SESE)
Decision date
2025-06-11
Date received
2024-09-17
Regulation
886.4670
Classification name
Unit, Phacofragmentation
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
N

Related Records

Applicant Contact

Contact
Andrew Rybold
Address
8740 Technology Way Reno NV US 89521 89521

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

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