Liquipette

FDA 510(k) K831079 · The Kendall Company Div. of Tyco Healthcare Group

Substantially Equivalent

510(k) numberK831079

Submission

Device name
Liquipette
Applicant
The Kendall Company Div. of Tyco Healthcare Group
Mchenry, IL, US
Received
April 4, 1983
Decision date
April 28, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GJG – Pipette, Quantitative, Hematology
Device class
Class I (low risk)
Regulation
21 CFR 864.6160
Specialty
Hematology

Other 510(k)s with product code GJG

510(k)DeviceApplicantDecision
K781891Pipettes, Plastic DisposableGJG · Traditional Hillwood Corp.11/15/1978SE
K780237Disposable Controlled Drop Pasteur PipetGJG · Traditional Owens-Illinois, Inc.03/09/1978SE
K760719Uniform Drop Size Pasteur Type PipetsGJG · Traditional Dade, Baxter Travenol Diagnostics, Inc.10/29/1976SE

More from Dade, Baxter Travenol Diagnostics, Inc.

510(k)DeviceDecision
K024010Dover Silver Hydrogel Coated Silicone Foley CatheterEZL · Traditional 06/11/2003SE
K831081Ezee Filter/SeparatorJKA · Traditional 05/16/1983SE
K831082Connecting TubingBYX · Traditional 05/09/1983SE

Questions and answers

When was Liquipette cleared by the FDA?

Liquipette (K831079) received a 510(k) decision of Substantially Equivalent on April 28, 1983, 24 days after the submission was received.

What is the product code of K831079?

The FDA product code is GJG – Pipette, Quantitative, Hematology, a Class I (low risk) device regulated under 21 CFR 864.6160.