ANTISERUM TO HUMAN IGM— 510(k) K790705

Unknown

Kent Laboratories, Inc.

FDA 510(k) clearance K790705 for ANTISERUM TO HUMAN IGM, Unknown on 1979-04-12. Applicant: Kent Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Kent Laboratories, Inc.
Product code: Code DAO
Device class: Class 2
Regulation: 21 CFR 866.5550
Advisory panel: Immunology
Date received: 1979-04-12
Decision date: 1979-04-12
Decision: Unknown
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.