Ivent Intravenous Adminstration Set

FDA 510(k) K852259 · Ivent Corp.

Substantially Equivalent

510(k) numberK852259

Submission

Device name
Ivent Intravenous Adminstration Set
Applicant
Ivent Corp.
Carlsbad, CA, US
Received
May 24, 1985
Decision date
June 7, 1985
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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Questions and answers

When was Ivent Intravenous Adminstration Set cleared by the FDA?

Ivent Intravenous Adminstration Set (K852259) received a 510(k) decision of Substantially Equivalent on June 7, 1985, 14 days after the submission was received.

What is the product code of K852259?

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