CORNING BLOOD COLLECTION CAPILLARY TUBES— 510(k) K850806

Name: FDA 510(k) clearance K850806
Creator: U.S. Food and Drug Administration
Published: 1985-03-25

Substantially Equivalent

Corning Medical & Scientific

FDA 510(k) clearance K850806 for CORNING BLOOD COLLECTION CAPILLARY TUBES, Substantially Equivalent on 1985-03-25. Applicant: Corning Medical & Scientific. Device class: 1.

Clearance details

Applicant: Corning Medical & Scientific
Product code: Code GIO
Device class: Class 1
Regulation: 21 CFR 864.6150
Advisory panel: Hematology
Date received: 1985-02-27
Decision date: 1985-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Medfield, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GIO

view all

K972969 — QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM1997-09-22
K941291 — MONOJECT SAMPLETTE SEPARATOR TUBE1994-10-27
K894851 — TRU-TRAX1989-09-29
K885324 — HEMA(PRO)TEC(TION)1989-02-17
K885138 — CAPILLARY TUBE, BLOOD COLLECTION1989-02-07

More clearances from Corning Medical & Scientific

view all

K875122 — DISPOSABLE STERILE SYRINGE FILTERS1988-01-12
K872273 — CORNING EASY WASH ELISA PLATES1987-07-07
K872076 — CORNING DISPOSABLE ROLLER BOTTLES1987-06-15
K863789 — CORNING ELISA PLATES1986-10-03
K854024 — CORNING MAGIC MAB HCG RADIOIMMUNOASSAY1985-11-26

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