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Cabinet, Instrument, Ac-Powered, Ophthalmic

HRE · Class I — Low Risk (general controls) · Ophthalmic · 21 CFR 886.1860

Classification

FDA Product Code

HRE

Device class

Class I — Low Risk (general controls)

Regulation

21 CFR 886.1860

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

0

Registered establishments

9

Source

Authoritative

FDA Device Classification database

Machine

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