CATALOG #4-2520 CHLORIDOMETER CHLORIDE— 510(k) K791312

Name: FDA 510(k) clearance K791312
Creator: U.S. Food and Drug Administration
Published: 1979-08-16

Substantially Equivalent

Buchler Instruments, Inc.

FDA 510(k) clearance K791312 for CATALOG #4-2520 CHLORIDOMETER CHLORIDE, Substantially Equivalent on 1979-08-16. Applicant: Buchler Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Buchler Instruments, Inc.
Product code: Code JIT
Device class: Class 2
Regulation: 21 CFR 862.1150
Advisory panel: Clinical Chemistry
Date received: 1979-07-11
Decision date: 1979-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JIT

view all

K171168 — VITROS Immunodiagnostic Products Insulin Calibrators2017-05-16
K170938 — CalSet IGF-12017-04-26
K170160 — Abbott ARCHITECT Free T32017-02-15
K163534 — Lumipulse G FSH-N Calibrators2017-01-13
K163546 — Lumipulse G Progesterone-N Calibrators2017-01-13

More clearances from Buchler Instruments, Inc.

view all

K760506 — HEMAFLOUR ZP1976-10-28

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