510(k) K230858

Device
QUATERA 700
Applicant
Carl Zeiss Meditec, AG
510(k) number
K230858
Product code
HQC
Decision
Substantially Equivalent (SESE)
Decision date
2023-07-31
Date received
2023-03-29
Regulation
886.4670
Classification name
Unit, Phacofragmentation
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Hans-Joachim Miesner
Address
Goeschwitzer Strasse 51-52 Jena DE 07745 07745

FDA Registration Numbers

Source Documents

510(k) summary PDF

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