FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulse

K Number: K231011 · Decision Sep 12, 2023
Classifications
1
FEI Numbers
60
Registration Numbers
61
Same Product Code
179
Applicant Total
6
Review Days
155

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Basic Information

Device Name
Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulse
K Number
K231011
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4390
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Meridian AG
Date Received
April 10, 2023
Decision Date
September 12, 2023
Product Code
HQF
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
HQF Laser, Ophthalmic

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Other Clearances by Meridian AG

K Number Device Name
K232417 MR Q; MR Q SUPINE; MR Q SLT
K160677 MICRORUPTOR 6
K113390 LASER INDIRECT OPHTHALMOSCOPE 500(LIO-500)
K072823 MERILAS 532A
K023045 MICRORUPTER V