FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

QUATERA 700

K Number: K230858 · Decision Jul 31, 2023
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
315
Applicant Total
45
Review Days
124

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Basic Information

Device Name
QUATERA 700
K Number
K230858
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4670
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Carl Zeiss Meditec, AG
Date Received
March 29, 2023
Decision Date
July 31, 2023
Product Code
HQC
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
HQC Unit, Phacofragmentation

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HQC), ordered by most recent decision date.

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Other Clearances by Carl Zeiss Meditec, AG

K Number Device Name
K241174 INTRABEAM (700); And accessories (INTRABEAM SMART Stand, INTRABEAM SMART Spherical Applicator, INTRABEAM Spherical Sizer Set, INTRABEAM Needle Applicator)
K233911 VISULAS combi
K240215 BLUE 400; BLUE 400 S
K233421 RESCAN 700
K232944 CALLISTO eye
K232159 QEVO System
K231676 CALLISTO eye
K213527 FORUM
K211346 BLUE 400
K212241 QUATERA 700
Search all 45 clearances from Carl Zeiss Meditec, AG →