Single Use 3-LUMEN Extraction Balloon V, Model V B-V233P-A,B-V233P-B,B-V433P-A,B-V433P-B, BV243Q-A, B-V243Q-B, B-V443Q-A

FDA 510(k) K091495 · Olympus Medical Systems Corporation

Substantially Equivalent

510(k) numberK091495

Submission

Device name
Single Use 3-LUMEN Extraction Balloon V, Model V B-V233P-A,B-V233P-B,B-V433P-A,B-V433P-B, BV243Q-A, B-V243Q-B, B-V443Q-A
Applicant
Olympus Medical Systems Corporation
Center Valley, PA, US
Received
May 20, 2009
Decision date
September 3, 2009
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LQR – Dislodger, Stone, Biliary
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5010
Specialty
Gastroenterology, Urology

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Questions and answers

When was Single Use 3-LUMEN Extraction Balloon V, Model V B-V233P-A,B-V233P-B,B-V433P-A,B-V433P-B, BV243Q-A, B-V243Q-B, B-V443Q-A cleared by the FDA?

Single Use 3-LUMEN Extraction Balloon V, Model V B-V233P-A,B-V233P-B,B-V433P-A,B-V433P-B, BV243Q-A, B-V243Q-B, B-V443Q-A (K091495) received a 510(k) decision of Substantially Equivalent on September 3, 2009, 106 days after the submission was received.

What is the product code of K091495?

The FDA product code is LQR – Dislodger, Stone, Biliary, a Class II (moderate risk) device regulated under 21 CFR 876.5010.