FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

DRSplus

K Number: K213705 · Decision Dec 21, 2021
Classifications
1
FEI Numbers
13
Registration Numbers
14
Same Product Code
21
Applicant Total
13
Review Days
27

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Basic Information

Device Name
DRSplus
K Number
K213705
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
886.1570
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Centervue S.P.A.
Date Received
November 24, 2021
Decision Date
December 21, 2021
Product Code
MYC
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
MYC Ophthalmoscope, Laser, Scanning

Similar 510(k) Clearances

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

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Other Clearances by Centervue S.P.A.

K Number Device Name
K243504 MAIA (AHMACME001)
K234076 iCare ALTIUS CW
K211328 EIDON FA, EIDON, EIDON AF, EIDON UWFL
K192113 DRSplus
K180526 EIDON FA
K180293 Retia 2
K153181 MAIA
K150320 COMPASS
K142047 EIDON
K133758 CENTERVUE MACULAR INTEGRITY ASSESSMENT
Search all 13 clearances from Centervue S.P.A. →