← FDA Medical Device Classifications

System, Therapeutic, X-Ray

JAD · Class II — Moderate Risk (510(k) clearance required) · Radiology · 21 CFR 892.5900

Classification

FDA Product Code

JAD

Device class

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

Regulation

21 CFR 892.5900

Review panel

RA

Medical specialty

Radiology

Submission type

1

GMP exempt

N

Life sustaining

N

Implant

N

Third-party review

N

Market data

Cleared 510(k) submissions

53

Registered establishments

20

Source

Authoritative

FDA Device Classification database

Machine

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