Single Use Aspiration Needle NA-U200H

FDA 510(k) K180449 · Olympus Medical Systems Corp.

Substantially Equivalent

510(k) numberK180449

Submission

Device name
Single Use Aspiration Needle NA-U200H
Applicant
Olympus Medical Systems Corp.
Hachioji-Shi, JP
Received
February 20, 2018
Decision date
June 8, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FCG – Biopsy Needle
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1075
Specialty
Gastroenterology, Urology

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Questions and answers

When was Single Use Aspiration Needle NA-U200H cleared by the FDA?

Single Use Aspiration Needle NA-U200H (K180449) received a 510(k) decision of Substantially Equivalent on June 8, 2018, 108 days after the submission was received.

What is the product code of K180449?

The FDA product code is FCG – Biopsy Needle, a Class II (moderate risk) device regulated under 21 CFR 876.1075.