Med-Rx Extension Sets

FDA 510(k) K990777 · Benlan, Inc.

Substantially Equivalent

510(k) numberK990777

Submission

Device name
Med-Rx Extension Sets
Applicant
Benlan, Inc.
Oakville, CA
Received
March 9, 1999
Decision date
August 25, 1999
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.

510(k)DeviceDecision
K131183Med-Rx Oral/Enteral SyringeKNT · Traditional 06/03/2014SE
K120375Med-Rx Patient Delivery SetFPA · Traditional 06/28/2012SE
K112799Med-Rx Extension Set with T-ConnectorFPA · Traditional 12/23/2011SE
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

Questions and answers

When was Med-Rx Extension Sets cleared by the FDA?

Med-Rx Extension Sets (K990777) received a 510(k) decision of Substantially Equivalent on August 25, 1999, 169 days after the submission was received.

What is the product code of K990777?

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