Chemotherapy Container

FDA 510(k) K911576 · Bemis Mfg. Co.

Substantially Equivalent

510(k) numberK911576

Submission

Device name
Chemotherapy Container
Applicant
Bemis Mfg. Co.
Sheboygan Falls, WI, US
Received
April 8, 1991
Decision date
July 5, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KPE – Container, I.V.
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5025
Specialty
General Hospital

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More from Gilero, LLC

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K020921No-Pokes Needle Safety DeviceFMI · Traditional 07/11/2002SE
K965248Bemis Two Gallon Sharps ContainerFMI · Traditional 02/14/1997SE
K964858Bemis Two Gallon Chemotherapy ContainerMMK · Traditional 02/11/1997SE
K960525Bemis One Quart Phlebotomy Container (Part Number 100)MMK · Traditional 03/28/1996SE
K953797Sharps Disposal ContainersMMK · Traditional 11/27/1995SE
K950340Ight and Eleven Gallon Sharps and Chemotherapy ContainersMMK · Traditional 06/02/1995SE
K941665Sharps Disposal Container/PhlebotomyMMK · Traditional 05/23/1994SE
K941664Sharp Disposal Containers Wall SafeMMK · Traditional 05/23/1994SE
K931664Sharps Disposable ContainersMMK · Traditional 05/23/1994SE
K914601Suction Connecting TubingGCX · Traditional 02/07/1992SE

Questions and answers

When was Chemotherapy Container cleared by the FDA?

Chemotherapy Container (K911576) received a 510(k) decision of Substantially Equivalent on July 5, 1991, 88 days after the submission was received.

What is the product code of K911576?

The FDA product code is KPE – Container, I.V., a Class II (moderate risk) device regulated under 21 CFR 880.5025.