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FDA 510(k)

Endoscopic Ultrasound Aspiration Needle

K-Number: K172309 · 2017-09-29

ApplicantMicro-Tech (Nanjing) Co., Ltd.
Decision Date2017-09-29
Product CodeODG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Endoscopic Ultrasound Aspiration Needle is a medical device manufactured by Micro-Tech (Nanjing) Co., Ltd.. It received FDA 510(k) clearance on 2017-09-29 under approval number K172309. The device is classified under product code ODG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Endoscopic Ultrasound Aspiration Needle?

Endoscopic Ultrasound Aspiration Needle is a medical device that received FDA 510(k) clearance on 2017-09-29. It is manufactured by Micro-Tech (Nanjing) Co., Ltd.. The 510(k) number is K172309.

When was Endoscopic Ultrasound Aspiration Needle approved by the FDA?

Endoscopic Ultrasound Aspiration Needle received FDA 510(k) clearance on 2017-09-29, under approval number K172309.

What company makes Endoscopic Ultrasound Aspiration Needle?

Endoscopic Ultrasound Aspiration Needle is manufactured by Micro-Tech (Nanjing) Co., Ltd..

What is the FDA product code for Endoscopic Ultrasound Aspiration Needle?

The FDA product code for Endoscopic Ultrasound Aspiration Needle is ODG.

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Related Devices (Code: ODG)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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