AUTOMATED SLIDE SPINNER— 510(k) K771898

Name: FDA 510(k) clearance K771898
Creator: U.S. Food and Drug Administration
Published: 1977-10-18

Substantially Equivalent

Dynatech Cryomedical Co.

FDA 510(k) clearance K771898 for AUTOMATED SLIDE SPINNER, Substantially Equivalent on 1977-10-18. Applicant: Dynatech Cryomedical Co.. Device class: 1.

Clearance details

Applicant: Dynatech Cryomedical Co.
Product code: Code GKJ
Device class: Class 1
Regulation: 21 CFR 864.5850
Advisory panel: Hematology
Date received: 1977-10-06
Decision date: 1977-10-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GKJ

view all

K854962 — MICRO-MAT SYSTEM1985-12-23
K854121 — MICRO-MAT SYSTEM1985-10-31
K831558 — E-Z PREP1983-06-16
K811534 — HEMASPINNER1981-08-18
K760007 — BLOOD-SMEARING INSTRUMENT (MINIPREP TM)1976-09-03

More clearances from Dynatech Cryomedical Co.

view all

K771815 — SIGMOSCOPE1977-10-07
K770896 — COLPOSCOPE MODEL II1977-06-03
K770614 — MONITOR, GAS MANIFOLD1977-04-07
K761205 — DYNATECH JD7/JD7P COLPOSCOPE1976-12-17
K760763 — COLPOSCOPE (DYNATECH COLPOSCOPE-MODEL I1976-10-20

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