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HIX · Class I — Low Risk (general controls) · Ophthalmic · 21 CFR 886.1435

Classification

FDA Product Code

HIX

Device class

Class I — Low Risk (general controls)

Regulation

21 CFR 886.1435

Review panel

OP

Medical specialty

Ophthalmic

Submission type

4

GMP exempt

N

Life sustaining

N

Implant

N

Third-party review

N

Market data

Cleared 510(k) submissions

2

Registered establishments

1

Source

Authoritative

FDA Device Classification database

Machine

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