BECKMAN CHOLINESTERASE REAGENT KIT— 510(k) K893583

Substantially Equivalent

Beckman

FDA 510(k) clearance K893583 for BECKMAN CHOLINESTERASE REAGENT KIT, Substantially Equivalent on 1989-08-15. Applicant: Beckman. Device class: 1.

Clearance details

Applicant: Beckman
Product code: Code DIH
Device class: Class 1
Regulation: 21 CFR 862.3240
Advisory panel: Clinical Toxicology
Date received: 1989-05-09
Decision date: 1989-08-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brea, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Beckman

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K971534 — SYNCHRON SYUSTEMS DAT DRUG FREE URINE CONTROL1997-05-21
K935362 — P-AMYLASE CONTROL1994-01-27
K904219 — SYNCHRON CX 7 CLINICAL ANALYZER1990-10-22
K904220 — SYNCHRON CX4-CE1990-10-15

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