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EAQ · Class II — Moderate Risk (510(k) clearance required) · Dental · 21 CFR 872.6350

Classification

FDA Product Code

EAQ

Device class

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

Regulation

21 CFR 872.6350

Review panel

DE

Medical specialty

Dental

Submission type

1

GMP exempt

N

Life sustaining

N

Implant

N

Third-party review

Y

Market data

Cleared 510(k) submissions

2

Registered establishments

4

Source

Authoritative

FDA Device Classification database

Machine

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