4 Low Volume IV Extension Set with Slide Clamp

FDA 510(k) K905218 · Marquette Medical, Inc.

Substantially Equivalent

510(k) numberK905218

Submission

Device name
4 Low Volume IV Extension Set with Slide Clamp
Applicant
Marquette Medical, Inc.
Crofton, MD, US
Received
November 20, 1990
Decision date
June 4, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FPA – Set, Administration, Intravascular
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

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More from B.Braun Medical, Inc.

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K021471Marquette Huber Trap Safety Infusion SetFPA · Traditional 09/08/2003SE
K953008Infant Feeding TubeFPD · Traditional 01/11/1996SE
K952976Plastic Blunt CannulaFPA · Traditional 09/15/1995SE
K920537Subcutaneous Infusion SetFPA · Traditional 10/13/1992SE
K9052194' Low Volume IV Extension SetFPA · Traditional 06/04/1991SE
K905374IV Extension Sets with .22 Micron FilterFPA · Traditional 05/31/1991SE
K901089Low Volume Trifurcated IV Extension SetFPA · Traditional 10/04/1990SE
K901088Low Volume Bifurcated IV Extension SetFPA · Traditional 10/04/1990SE
K900427IV Trifurcated Extension SetFPA · Traditional 02/28/1990SE
K900426IV Bifurcated Extension SetFPA · Traditional 02/28/1990SE

Questions and answers

When was 4 Low Volume IV Extension Set with Slide Clamp cleared by the FDA?

4 Low Volume IV Extension Set with Slide Clamp (K905218) received a 510(k) decision of Substantially Equivalent on June 4, 1991, 196 days after the submission was received.

What is the product code of K905218?

The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.