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Substance, Blood Grouping Of Non-Human Origin For In Vitro Diagnostic Use

KSX · Class II — Moderate Risk (510(k) clearance required) · Hematology · 21 CFR 864.9160

Classification

FDA Product Code

KSX

Device class

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

Regulation

21 CFR 864.9160

Review panel

HE

Medical specialty

Hematology

Submission type

4

GMP exempt

N

Life sustaining

N

Implant

N

Third-party review

N

Market data

Cleared 510(k) submissions

8

Registered establishments

5

Source

Authoritative

FDA Device Classification database

Machine

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