← FDA Medical Device Classifications

Goniometer, Nonpowered

KQW · Class I — Low Risk (general controls) · Orthopedic · 21 CFR 888.1520

Classification

FDA Product Code

KQW

Device class

Class I — Low Risk (general controls)

Regulation

21 CFR 888.1520

Review panel

NE

Medical specialty

Orthopedic

Submission type

4

GMP exempt

N

Life sustaining

N

Implant

N

Third-party review

N

Market data

Cleared 510(k) submissions

13

Registered establishments

83

Source

Authoritative

FDA Device Classification database

Machine

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