NM Injection Needles

FDA 510(k) K902736 · Olympus Corp.

Substantially Equivalent

510(k) numberK902736

Submission

Device name
NM Injection Needles
Applicant
Olympus Corp.
Lake Success, NY, US
Received
June 21, 1990
Decision date
August 24, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FBK – Endoscopic Injection Needle, Gastroenterology-Urology
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

inserted through endoscope for injection of a solution, gas, or implantable materials into gi or gu tissue.

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Questions and answers

When was NM Injection Needles cleared by the FDA?

NM Injection Needles (K902736) received a 510(k) decision of Substantially Equivalent on August 24, 1990, 64 days after the submission was received.

What is the product code of K902736?

The FDA product code is FBK – Endoscopic Injection Needle, Gastroenterology-Urology, a Class II (moderate risk) device regulated under 21 CFR 876.1500.