← FDA Medical Device Classifications

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INI · Class II — Moderate Risk (510(k) clearance required) · Physical Medicine · 21 CFR 890.3800

Classification

FDA Product Code
INI
Device class
Class II — Moderate Risk (510(k) clearance required)
Regulation
21 CFR 890.3800
Review panel
PM
Medical specialty
Physical Medicine
Submission type
1
GMP exempt
N
Life sustaining
N
Implant
N
Third-party review
Y

Market data

Cleared 510(k) submissions
344
Registered establishments
67

Source

Authoritative
FDA Device Classification database
Machine
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