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FDA 510(k)

BARD ENDOSCOPIC OVERTUBE

K-Number: K942044 · 1994-06-10

ApplicantC.R. Bard, Inc.
Decision Date1994-06-10
Product CodeFED
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BARD ENDOSCOPIC OVERTUBE is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1994-06-10 under 510(k) number K942044. The device is classified under product code FED. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD ENDOSCOPIC OVERTUBE?

BARD ENDOSCOPIC OVERTUBE is a medical device that received FDA 510(k) clearance on 1994-06-10. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K942044.

When did BARD ENDOSCOPIC OVERTUBE receive FDA 510(k) clearance?

BARD ENDOSCOPIC OVERTUBE received FDA 510(k) clearance on 1994-06-10, under 510(k) number K942044.

Who is the listed applicant for BARD ENDOSCOPIC OVERTUBE?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARD ENDOSCOPIC OVERTUBE?

The FDA product code for BARD ENDOSCOPIC OVERTUBE is FED.

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Related Devices (Code: FED)

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K260512Disposable Ureteral Access SheathYangzhou Fartley Medical Instrument Technology Co., Ltd.K262262Pathfinder Endoscope OvertubeNeptune Medical, Inc.K260410Single Use Ureteral Access SheathZhejiang Chuangxiang Medical Technology Co., Ltd.K261915Navigator™ Flex Ureteral Access Sheath SetBoston Scientific CorporationK260965CVAC Aspiration SystemCalyxo, Inc.K260521ClearEVAC Ureteral Aspirating Access Sheath (PUS-100-1040,PUS-100-1050, PUS-100-1240,PUS-100-1250)Zhuhai Pusen Medical Technology Co., 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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