QUICK STAIN WRIGHT'S GIEMSA W/BUFF— 510(k) K833677

Name: FDA 510(k) clearance K833677
Creator: U.S. Food and Drug Administration
Published: 1983-11-25

Substantially Equivalent

J.S. Medical Assoc.

FDA 510(k) clearance K833677 for QUICK STAIN WRIGHT'S GIEMSA W/BUFF, Substantially Equivalent on 1983-11-25. Applicant: J.S. Medical Assoc.. Device class: 1.

Clearance details

Applicant: J.S. Medical Assoc.
Product code: Code HYF
Device class: Class 1
Regulation: 21 CFR 864.1850
Advisory panel: Hematology
Date received: 1983-10-18
Decision date: 1983-11-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HYF

view all

K842742 — GIEMSA STAIN1984-08-15
K833665 — HEMATOLOGY WRIGHT'S-GIEMSA SATIN PACK1983-11-25
K831131 — CASE WRIGHT-GIEMSA STAIN PAK1983-06-08

More clearances from J.S. Medical Assoc.

view all

K932752 — VISI-SPOT1993-11-05
K932688 — EYE SPOT IM TEST1993-09-08
K932180 — EYE SPOT CRP TEST1993-08-23
K932551 — ACCUTEX IM LATEX TEST1993-08-09
K926112 — ACCUTEX BETA-HCG TEST1993-07-28

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