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FDA 510(k)

DISPOSABLE ASPIRATION NEEDLE NA-200H

K-Number: K023272 · 2002-12-23

ApplicantThe Olympus Optical Co.
Decision Date2002-12-23
Product CodeFCG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE ASPIRATION NEEDLE NA-200H is the device name listed in this FDA 510(k) record. The listed applicant is The Olympus Optical Co.. It received FDA 510(k) clearance on 2002-12-23 under 510(k) number K023272. The device is classified under product code FCG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE ASPIRATION NEEDLE NA-200H?

DISPOSABLE ASPIRATION NEEDLE NA-200H is a medical device that received FDA 510(k) clearance on 2002-12-23. The listed applicant is The Olympus Optical Co.. The 510(k) number is K023272.

When did DISPOSABLE ASPIRATION NEEDLE NA-200H receive FDA 510(k) clearance?

DISPOSABLE ASPIRATION NEEDLE NA-200H received FDA 510(k) clearance on 2002-12-23, under 510(k) number K023272.

Who is the listed applicant for DISPOSABLE ASPIRATION NEEDLE NA-200H?

The FDA 510(k) record lists The Olympus Optical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE ASPIRATION NEEDLE NA-200H?

The FDA product code for DISPOSABLE ASPIRATION NEEDLE NA-200H is FCG.

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Other records listing The Olympus Optical Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K032066SONOSURG SYSTEMK030194XUES-41 ENDOSCOPIC ELECTROSURGICAL UNITK021962OLYMPUS ULTRASONIC SURGICAL SYSTEMK023984MODIFICATION TO OLYMPUS BRONCHOSCOPES BF-40 SERIES, BF-240 SERIES, AND BF-160 SERIESK023767UES-30 ELECTROSURGICAL UNIT AND IT'S ASSOCIATED ACCESSORIESK012074XBO1-824-18/19/20 BIOPSY FORCEPS

View all 22 devices →

Related Devices (Code: FCG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252646Single-Use Fine Needle Biopsy (FNB) device (NA-U210H)Olympus Medical Systems Corp.K250994ClearTip FNA and FNB TypesFinemedix Co., Ltd.K241209EchoTip AcuCore™ EUS Biopsy Needle (ECHO-BX-19)Cook Ireland, Ltd.K231422Precision GILimaca Medical, Ltd.K231267ClearTipFinemedix Co., Ltd.K230909EchoTip® AcuCore™ Ultrasound Biopsy Needle (ECHO-BX-3-22)Cook Ireland, Ltd.

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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