TRISACRYL GF 05 & TRISACRYL GF 2000— 510(k) K840985

Name: FDA 510(k) clearance K840985
Creator: U.S. Food and Drug Administration
Published: 1984-04-19

Substantially Equivalent

Lkb Instruments, Inc.

FDA 510(k) clearance K840985 for TRISACRYL GF 05 & TRISACRYL GF 2000, Substantially Equivalent on 1984-04-19. Applicant: Lkb Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Lkb Instruments, Inc.
Product code: Code DJY
Device class: Class 1
Regulation: 21 CFR 862.2230
Advisory panel: Clinical Chemistry
Date received: 1984-03-07
Decision date: 1984-04-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DJY

view all

K890113 — THE CDI(R) SYSTEM 4001989-05-23
K883615 — LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/731988-12-16
K881361 — SOLID PHASE EXTRACTION TUBES1988-08-08
K850963 — DUPONT PREP TYPE SI EXTRACITON CARTRIDGE1985-03-25
K832198 — HC40/HC75 PREPACKED COLUMS1983-08-12

More clearances from Lkb Instruments, Inc.

view all

K874094 — 1205 BETAPLATE LIQUID SCINTILLATION COUNTER1987-11-04
K872955 — DELFIA(TM) FERRITIN KIT1987-08-21
K871303 — DELFIA(TM) THYROXINE (T4) KIT1987-06-17
K871599 — DELFIA(TM) HIGE KIT1987-06-12
K871644 — DELFIA (TM) HTSH KIT1987-05-12

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