Effectiv (TM) Cap

FDA 510(k) K080579 · Hospira, Inc.

Substantially Equivalent

510(k) numberK080579

Submission

Device name
Effectiv (TM) Cap
Applicant
Hospira, Inc.
Lake Forest, IL, US
Received
March 3, 2008
Decision date
September 11, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
QBP – Cap, Device Disinfectant
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

Disinfect needleless access valves and may act as a physical barrier to contamination if not removed for a set period of time

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K143612LifeCare PCA Infusion SystemMEA · Traditional 04/08/2016SE
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Questions and answers

When was Effectiv (TM) Cap cleared by the FDA?

Effectiv (TM) Cap (K080579) received a 510(k) decision of Substantially Equivalent on September 11, 2008, 192 days after the submission was received.

What is the product code of K080579?

The FDA product code is QBP – Cap, Device Disinfectant, a Class II (moderate risk) device regulated under 21 CFR 880.5440.