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IRT · Class II — Moderate Risk (510(k) clearance required) · Physical Medicine · 21 CFR 890.5740

Classification

FDA Product Code
IRT
Device class
Class II — Moderate Risk (510(k) clearance required)
Regulation
21 CFR 890.5740
Review panel
PM
Medical specialty
Physical Medicine
Submission type
4
GMP exempt
N
Life sustaining
N
Implant
N
Third-party review
N

Market data

Cleared 510(k) submissions
42
Registered establishments
253

Source

Authoritative
FDA Device Classification database
Machine
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