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MMK · Class II — Moderate Risk (510(k) clearance required) · General Hospital · 21 CFR 880.5570

Classification

FDA Product Code

MMK

Device class

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

Regulation

21 CFR 880.5570

Review panel

HO

Medical specialty

General Hospital

Submission type

1

GMP exempt

N

Life sustaining

N

Implant

N

Third-party review

Y

Market data

Cleared 510(k) submissions

112

Registered establishments

91

Source

Authoritative

FDA Device Classification database

Machine

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