MRI PROLACTIN RIA KIT— 510(k) K810949

Name: FDA 510(k) clearance K810949
Creator: U.S. Food and Drug Administration
Published: 1981-07-10

Substantially Equivalent

Microanalytic Research, Inc.

FDA 510(k) clearance K810949 for MRI PROLACTIN RIA KIT, Substantially Equivalent on 1981-07-10. Applicant: Microanalytic Research, Inc.. Device class: 1.

Clearance details

Applicant: Microanalytic Research, Inc.
Product code: Code CFT
Device class: Class 1
Regulation: 21 CFR 862.1625
Advisory panel: Clinical Chemistry
Date received: 1981-04-07
Decision date: 1981-07-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CFT

view all

K971921 — PROLACTIN (PRL) HORMONE MICROPLATE ELISA1997-06-24
K970281 — VITROS IMMUNODIAGNOSTIC PRODUCTS PROLACTIN REAGENT PACK/CALIBRATORS1997-02-25
K970188 — SEALITE SCIENCES, INC. AQUALITE PROLACTIN1997-02-20
K964748 — ELECSYS PROLACTIN ASSAY1997-01-21
K960561 — DSL ACTIVE PROLACTIN ELISA MODEL 10-45001996-04-26

More clearances from Microanalytic Research, Inc.

view all

K861097 — TRYPSIN RIA KIT1986-05-29
K820741 — MR1 LUTROPIN RIA KIT1982-04-14
K820740 — MR1 FOLLITROPIN RIA KIT1982-04-06
K813516 — MRI TOBRAMYCIN RIA KIT1981-12-29
K812394 — MRI GENTAMICIN RIA KIT1981-09-08

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