← FDA Medical Device Classifications

Stages, Microscope

KEJ · Class I — Low Risk (general controls) · Pathology · 21 CFR 864.3600

Classification

FDA Product Code

KEJ

Device class

Class I — Low Risk (general controls)

Regulation

21 CFR 864.3600

Review panel

PA

Medical specialty

Pathology

Submission type

4

GMP exempt

Y

Life sustaining

N

Implant

N

Third-party review

N

Market data

Cleared 510(k) submissions

1

Registered establishments

3

Source

Authoritative

FDA Device Classification database

Machine

JSON-LD · Markdown