HPL RIA KIT— 510(k) K790919

Substantially Equivalent

Technia Diagnostics , Ltd.

FDA 510(k) clearance K790919 for HPL RIA KIT, Substantially Equivalent on 1979-06-28. Applicant: Technia Diagnostics , Ltd.. Device class: 2.

Clearance details

Applicant: Technia Diagnostics , Ltd.
Product code: Code JMF
Device class: Class 2
Regulation: 21 CFR 862.1585
Advisory panel: Clinical Chemistry
Date received: 1979-05-14
Decision date: 1979-06-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JMF

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K823292 — IMMOPHASE TM HPL RADIOIMMUNOASSAY1982-12-28
K823201 — HUMAN PLACENTAL LACTOGEN KIT1982-11-29
K811370 — NATAL-TEC HPL1981-05-29

More clearances from Technia Diagnostics , Ltd.

K861978 — AUTOFLUOR V1986-06-10
K801843 — T3(125) RADIOIMMUNOASSAY KIT1980-09-16
K801202 — DIGOXIN RADIOIMMUNOASSAY KIT1980-06-20
K801203 — CORTISOL RADIOIMMUNOASSAY KIT1980-06-09
K791361 — T3 UPTAKE RADIOIMMUNOASSAY KIT1979-08-16

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