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FDA 510(k)

Expect Slimline (SL) Endoscopic Ultrasound Aspiration Needle

K-Number: K173184 · 2017-10-27

ApplicantBoston Scientific
Decision Date2017-10-27
Product CodeODG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Expect Slimline (SL) Endoscopic Ultrasound Aspiration Needle is a medical device manufactured by Boston Scientific. It received FDA 510(k) clearance on 2017-10-27 under approval number K173184. 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 Expect Slimline (SL) Endoscopic Ultrasound Aspiration Needle?

Expect Slimline (SL) Endoscopic Ultrasound Aspiration Needle is a medical device that received FDA 510(k) clearance on 2017-10-27. It is manufactured by Boston Scientific. The 510(k) number is K173184.

When was Expect Slimline (SL) Endoscopic Ultrasound Aspiration Needle approved by the FDA?

Expect Slimline (SL) Endoscopic Ultrasound Aspiration Needle received FDA 510(k) clearance on 2017-10-27, under approval number K173184.

What company makes Expect Slimline (SL) Endoscopic Ultrasound Aspiration Needle?

Expect Slimline (SL) Endoscopic Ultrasound Aspiration Needle is manufactured by Boston Scientific.

What is the FDA product code for Expect Slimline (SL) Endoscopic Ultrasound Aspiration Needle?

The FDA product code for Expect Slimline (SL) Endoscopic Ultrasound Aspiration Needle is ODG.

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Related Devices (Code: ODG)

K160845Acquire Endoscopic Ultrasound Fine Needle Biopsy (FNB) DeviceBoston Scientific Corporation K172309Endoscopic Ultrasound Aspiration NeedleMicro-Tech (Nanjing) Co., Ltd. K162447PENTAX Medical Endoscopic Ultrasound System, EG-3270UK Upper G.I. Video Scope (Convex Array Type) with EPK-i5010 Video Processor and HI VISION Preirus Ultrasound ScannerPentax of America, Inc. K163058Expect Slimline (SL) Endoscopic Ultrasound Aspiration NeedleBoston Scientific K182004PENTAX Medical Endoscopic Ultrasound SystemPentax of America, Inc. K180731Ultramatrix EUS BalloonUnited States Endoscopy Group, Inc. (Us Endoscopy)

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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