← FDA Medical Device Classifications

Ultrasound, Sinus

LWI · Class II — Moderate Risk (510(k) clearance required) · Radiology · 21 CFR 892.1560

Classification

FDA Product Code

LWI

Device class

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

Regulation

21 CFR 892.1560

Review panel

EN

Medical specialty

Radiology

Submission type

1

GMP exempt

N

Life sustaining

N

Implant

N

Third-party review

N

Market data

Cleared 510(k) submissions

4

Registered establishments

0

Source

Authoritative

FDA Device Classification database

Machine

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