Med-Rx Patient Delivery Set

FDA 510(k) K120375 · Benlan, Inc.

Substantially Equivalent

510(k) numberK120375

Submission

Device name
Med-Rx Patient Delivery Set
Applicant
Benlan, Inc.
Oakville, CA
Received
February 6, 2012
Decision date
June 28, 2012
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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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K100700Med-Rx Pediatric Feeding Tubes and AccessoriesFPD · Traditional 12/13/2010SE
K102073Med-Rx Transfer Set, Models 10-1227TS, 10-1300TS, 10-1305TS and 10-1306TSFPA · Traditional 11/08/2010SE
K010607Med-Rx Irrigation Set, Model 10-3001, 10-3002, 10-4000, 10-4001LJH · Traditional 11/28/2001SE
K990777Med-Rx Extension SetsFPA · Traditional 08/25/1999SE

Questions and answers

When was Med-Rx Patient Delivery Set cleared by the FDA?

Med-Rx Patient Delivery Set (K120375) received a 510(k) decision of Substantially Equivalent on June 28, 2012, 143 days after the submission was received.

What is the product code of K120375?

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