← FDA Medical Device Classifications

Instrument, Coagulation

KQG · Class II — Moderate Risk (510(k) clearance required) · Hematology · 21 CFR 864.5400

Classification

FDA Product Code

KQG

Device class

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

Regulation

21 CFR 864.5400

Review panel

HE

Medical specialty

Hematology

Submission type

1

GMP exempt

N

Life sustaining

N

Implant

N

Third-party review

Y

Market data

Cleared 510(k) submissions

14

Registered establishments

4

Source

Authoritative

FDA Device Classification database

Machine

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