Manan Contrast Media Administration Set

FDA 510(k) K864405 · Manan Manufacturing Co., Inc.

Substantially Equivalent

510(k) numberK864405

Submission

Device name
Manan Contrast Media Administration Set
Applicant
Manan Manufacturing Co., Inc.
Skokie, IL, US
Received
November 10, 1986
Decision date
December 18, 1986
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.

510(k)DeviceDecision
K873208Manan Turner Style NeedleKNW · Traditional 08/25/1987SE
K863848Manan Brest Tumor Localization NeedleGAA · Traditional 10/14/1986SE
K852501Myelogram Procedure Tray · Traditional 07/11/1985SESD
K852018Arthrogram Tray for Double & Single Contrast Arthr · Traditional 07/11/1985SESD
K851834Manan Gwi Guide Wire IntroducerDWS · Traditional 07/11/1985SE
K851833Manan Seldinger NeedleDWS · Traditional 07/11/1985SE
K851832Naman Potts Cournand NeedleDWS · Traditional 07/11/1985SE
K852428Manan Epidural NeedleGCB · Traditional 06/27/1985SE
K852427Manan Spinal NeedleGAA · Traditional 06/27/1985SE
K852426Manan Trocar Style Biopsy NeedleGAA · Traditional 06/27/1985SE

Questions and answers

When was Manan Contrast Media Administration Set cleared by the FDA?

Manan Contrast Media Administration Set (K864405) received a 510(k) decision of Substantially Equivalent on December 18, 1986, 38 days after the submission was received.

What is the product code of K864405?

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