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IWI · Class II — Moderate Risk (510(k) clearance required) · Radiology · 21 CFR 892.5730

Classification

FDA Product Code

IWI

Device class

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

Regulation

21 CFR 892.5730

Review panel

RA

Medical specialty

Radiology

Submission type

1

GMP exempt

N

Life sustaining

N

Implant

N

Third-party review

Y

Market data

Cleared 510(k) submissions

6

Registered establishments

1

Source

Authoritative

FDA Device Classification database

Machine

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