AMIKACIN RIA KIT— 510(k) K802877

Substantially Equivalent

Antibodies, Inc.

FDA 510(k) clearance K802877 for AMIKACIN RIA KIT, Substantially Equivalent on 1980-12-19. Applicant: Antibodies, Inc.. Device class: 2.

Clearance details

Applicant: Antibodies, Inc.
Product code: Code KLQ
Device class: Class 2
Regulation: 21 CFR 862.3035
Advisory panel: Clinical Toxicology
Date received: 1980-11-17
Decision date: 1980-12-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KLQ

K052815 — QMS AMIKACIN REAGENTS2005-11-01
K033884 — RANDOX AMIKACIN2004-06-09
K955570 — INNOFLUOR AMIKACIN ASSAY SYSTEM1996-02-09
K903100 — INNOFLUOR (TM) AMIKACIN REAGENT SET1990-08-09
K894517 — FPR AMIKACIN KIT1989-09-28

More clearances from Antibodies, Inc.

K890774 — GIARDEIA(TM)1989-04-04
K843590 — DETECT-A-STREP1984-10-30
K822892 — CORTISOL RIA KIT1982-11-01
K812749 — ULTRA-DIG1981-10-19
K812314 — CRITHIDNA ANTI-DNA TEST KIT1981-09-01

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