ANTI-HUMAN LAMBDA SERUM— 510(k) K781220

Substantially Equivalent

Icl Scientific

FDA 510(k) clearance K781220 for ANTI-HUMAN LAMBDA SERUM, Substantially Equivalent on 1978-07-27. Applicant: Icl Scientific. Device class: 2.

Clearance details

Applicant: Icl Scientific
Product code: Code DEH
Device class: Class 2
Regulation: 21 CFR 866.5550
Advisory panel: Immunology
Date received: 1978-07-17
Decision date: 1978-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K832823 — ENZYMUNE-TEST TSH1983-10-14
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Data sourced from openFDA. This site is unofficial and independent of the FDA.