Q-CHECK REAGENT STANDARDS— 510(k) K830134

Substantially Equivalent

Lab Ability, Inc.

FDA 510(k) clearance K830134 for Q-CHECK REAGENT STANDARDS, Substantially Equivalent on 1983-01-09. Applicant: Lab Ability, Inc.. Device class: 1.

Clearance details

Applicant: Lab Ability, Inc.
Product code: Code LJG
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1983-01-09
Decision date: 1983-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LJG

K943228 — MICROSPORIDIUM CONTROL SET1994-10-27
K924893 — MICROSPORIDIUM CONTROL SLIDE1993-01-15
K890670 — CRYPTOSPORIDIUM CONTROL SLIDE1989-03-16
K890718 — GRAM STAIN CONTROL SLIDE1989-03-16
K890616 — BION DIRECT IDENTIFICATION CONTROL SLIDE1989-02-17

More clearances from Lab Ability, Inc.

K833407 — SELECTO-DISC NOVOBIOCIN 5UG1983-12-30
K832436 — SELECTRO-DISC1983-09-26
K830133 — Q-CHECK CULTI-LOOPS1983-02-09
K813191 — SHIGELLA SERA-CHEK1981-12-03

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