CERUOPLASMIN SERUM ANTI-HUMAN— 510(k) K781024

Substantially Equivalent

Icl Scientific

FDA 510(k) clearance K781024 for CERUOPLASMIN SERUM ANTI-HUMAN, Substantially Equivalent on 1978-08-14. Applicant: Icl Scientific. Device class: 2.

Clearance details

Applicant: Icl Scientific
Product code: Code DDB
Device class: Class 2
Regulation: 21 CFR 866.5210
Advisory panel: Immunology
Date received: 1978-06-19
Decision date: 1978-08-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code DDB

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K913668 — CAERULOPLASMIN IMMUNOLOGICAL NL TEST KIT1991-12-20

More clearances from Icl Scientific

K883942 — HYCOR SENTRY DRUGS OF ABUSE URINE CONTROL1988-11-10
K843565 — KOVA TROL I,II, III HUMAN URINE-DRIED1984-10-05
K833761 — THERAPEUTIC DRUG CONTROL1984-01-13
K832823 — ENZYMUNE-TEST TSH1983-10-14
K831383 — EVENT-TEST SLIDE1983-06-22

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