Van Dellen Bacteria Filter

FDA 510(k) K873465 · Van Dellen, Ltd.

Substantially Equivalent

510(k) numberK873465

Submission

Device name
Van Dellen Bacteria Filter
Applicant
Van Dellen, Ltd.
Tucson, AZ, US
Received
August 28, 1987
Decision date
January 20, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FPK – Tubing, Fluid Delivery
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

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More from Sysmex Corp.

510(k)DeviceDecision
K873464Van Dellen CannulaJOL · Traditional 11/23/1987SE
K873463Van Dellen Aspirating TubingBYY · Traditional 11/23/1987SE
K873462Van Dellen AspiratorBTA · Traditional 09/25/1987SE
K873164Van Dellen Healon CannulaHMX · Traditional 09/04/1987SE
K873163Van Dellen Irrigating CystotomeHNY · Traditional 09/04/1987SE
K873162Van Dellen Retrobulbar NeedleHMX · Traditional 09/04/1987SE

Questions and answers

When was Van Dellen Bacteria Filter cleared by the FDA?

Van Dellen Bacteria Filter (K873465) received a 510(k) decision of Substantially Equivalent on January 20, 1988, 145 days after the submission was received.

What is the product code of K873465?

The FDA product code is FPK – Tubing, Fluid Delivery, a Class II (moderate risk) device regulated under 21 CFR 880.5440.