Cellvizio 100 Series System and Cellvizio System with Confocal Miniprobes; Uroflex B and Cystolflex F (Both Trade Marked

FDA 510(k) K132389 · Daniel & Daniel Consulting

Substantially Equivalent

510(k) numberK132389

Submission

Device name
Cellvizio 100 Series System and Cellvizio System with Confocal Miniprobes; Uroflex B and Cystolflex F (Both Trade Marked
Applicant
Daniel & Daniel Consulting
Orinda, CA, US
Received
August 1, 2013
Decision date
February 25, 2014
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
OWN – Confocal Optical Imaging
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

Collection of light signals for visualization of cellular microstructures.

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Questions and answers

When was Cellvizio 100 Series System and Cellvizio System with Confocal Miniprobes; Uroflex B and Cystolflex F (Both Trade Marked cleared by the FDA?

Cellvizio 100 Series System and Cellvizio System with Confocal Miniprobes; Uroflex B and Cystolflex F (Both Trade Marked (K132389) received a 510(k) decision of Substantially Equivalent on February 25, 2014, 208 days after the submission was received.

What is the product code of K132389?

The FDA product code is OWN – Confocal Optical Imaging, a Class II (moderate risk) device regulated under 21 CFR 876.1500.