LYSING & HEMOGLOBIN S-REAGENT J & S— 510(k) K833444

Name: FDA 510(k) clearance K833444
Creator: U.S. Food and Drug Administration
Published: 1983-11-03

Substantially Equivalent

Jasins & Sayles Associates, Inc.

FDA 510(k) clearance K833444 for LYSING & HEMOGLOBIN S-REAGENT J & S, Substantially Equivalent on 1983-11-03. Applicant: Jasins & Sayles Associates, Inc.. Device class: 1.

Clearance details

Applicant: Jasins & Sayles Associates, Inc.
Product code: Code GGK
Device class: Class 1
Regulation: 21 CFR 864.8540
Advisory panel: Hematology
Date received: 1983-10-05
Decision date: 1983-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K863114 — PIASTRINIT1986-11-06

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K833443 — ISOTONIC BLOOD CELL DILUENT J & S1983-11-03

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