← FDA Medical Device Classifications

Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla

LXS · Class II — Moderate Risk (510(k) clearance required) · Ophthalmic · 21 CFR 886.4392

Classification

FDA Product Code

LXS

Device class

Class II — Moderate Risk (510(k) clearance required)

Regulation

21 CFR 886.4392

Review panel

OP

Medical specialty

Ophthalmic

Submission type

1

GMP exempt

N

Life sustaining

N

Implant

N

Third-party review

Y

Market data

Cleared 510(k) submissions

6

Registered establishments

3

Source

Authoritative

FDA Device Classification database

Machine

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