MEASELISA TEST KIT— 510(k) K821762

Substantially Equivalent

M.A. Bioproducts

FDA 510(k) clearance K821762 for MEASELISA TEST KIT, Substantially Equivalent on 1982-07-30. Applicant: M.A. Bioproducts. Device class: 1.

Clearance details

Applicant: M.A. Bioproducts
Product code: Code LJB
Device class: Class 1
Regulation: 21 CFR 866.3520
Advisory panel: Microbiology
Date received: 1982-06-15
Decision date: 1982-07-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LJB

K974552 — DIAMEDIX IS-MEASLES IGG TEST SYSTEM1998-01-28
K971620 — QUANTA LITE RUBEOLA (MEASLES) IGG1997-07-22
K922330 — BARTELS RUBEOLA IGG EIA1992-09-02
K922335 — BARTELS RUBEOLA IGM EIA1992-09-02
K910290 — VIRATEST-DIA(TM) MEASLES (RUBEOLA)1992-03-18

More clearances from M.A. Bioproducts

K822883 — HERPELISA KIT1983-07-26
K823804 — MYCOPLASMELISA TEST KIT1983-05-25
K830045 — MUMPSELISA TEST KIT1983-05-13
K830615 — CYTOMEGELISA STAT1983-05-09
K823805 — VARICELISA TEST KIT1983-05-05

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