LIQUIPETTE— 510(k) K831079

Name: FDA 510(k) clearance K831079
Creator: U.S. Food and Drug Administration
Published: 1983-04-28

Substantially Equivalent

The Kendall Company Div. of Tyco Healthcare Group

FDA 510(k) clearance K831079 for LIQUIPETTE, Substantially Equivalent on 1983-04-28. Applicant: The Kendall Company Div. of Tyco Healthcare Group. Device class: 1.

Clearance details

Applicant: The Kendall Company Div. of Tyco Healthcare Group
Product code: Code GJG
Device class: Class 1
Regulation: 21 CFR 864.6160
Advisory panel: Hematology
Date received: 1983-04-04
Decision date: 1983-04-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GJG

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K781891 — PIPETTES, PLASTIC DISPOSABLE1978-11-15
K780237 — DISPOSABLE CONTROLLED DROP PASTEUR PIPET1978-03-09
K760719 — UNIFORM DROP SIZE PASTEUR TYPE PIPETS1976-10-29

More clearances from The Kendall Company Div. of Tyco Healthcare Group

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K024010 — DOVER SILVER HYDROGEL COATED SILICONE FOLEY CATHETER2003-06-11
K831081 — EZEE FILTER/SEPARATOR1983-05-16
K831082 — CONNECTING TUBING1983-05-09

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