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FDA 510(k)

COAXIAL NEEDLE

K-Number: K971842 · 1997-06-20

ApplicantUnited States Endoscopy Group, Inc.
Decision Date1997-06-20
Product CodeFCG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

COAXIAL NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 1997-06-20 under 510(k) number K971842. 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 COAXIAL NEEDLE?

COAXIAL NEEDLE is a medical device that received FDA 510(k) clearance on 1997-06-20. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K971842.

When did COAXIAL NEEDLE receive FDA 510(k) clearance?

COAXIAL NEEDLE received FDA 510(k) clearance on 1997-06-20, under 510(k) number K971842.

Who is the listed applicant for COAXIAL NEEDLE?

The FDA 510(k) record lists United States Endoscopy Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COAXIAL NEEDLE?

The FDA product code for COAXIAL NEEDLE is FCG.

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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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