510(k) K230722

Device
Eagle device
Applicant
Belkin Vision, Ltd.
510(k) number
K230722
Product code
HQF
Decision
Substantially Equivalent (SESE)
Decision date
2023-12-08
Date received
2023-03-16
Regulation
886.4390
Classification name
Laser, Ophthalmic
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Daria Lemann-Blumenthal
Address
13 Gan Rave Blvd. Yavne IL 8122214 8122214

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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