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FDA 510(k)

MEMOTHERM COLORECTAL STENT

K-Number: K990504 · 2000-03-16

ApplicantC.R. Bard, Inc.
Decision Date2000-03-16
Product CodeMQR
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEMOTHERM COLORECTAL STENT 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 2000-03-16 under 510(k) number K990504. The device is classified under product code MQR. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEMOTHERM COLORECTAL STENT?

MEMOTHERM COLORECTAL STENT is a medical device that received FDA 510(k) clearance on 2000-03-16. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K990504.

When did MEMOTHERM COLORECTAL STENT receive FDA 510(k) clearance?

MEMOTHERM COLORECTAL STENT received FDA 510(k) clearance on 2000-03-16, under 510(k) number K990504.

Who is the listed applicant for MEMOTHERM COLORECTAL STENT?

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 MEMOTHERM COLORECTAL STENT?

The FDA product code for MEMOTHERM COLORECTAL STENT is MQR.

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Related Devices (Code: MQR)

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.

K234046WallFlex Colonic Stent System with Anchor Lock Delivery System; WallFlex Duodenal Stent System with Anchor Lock Delivery System; WallFlex Colonic Soft Stent System with Anchor Lock Delivery System; WallFlex Duodenal Soft Stent System with Anchor Lock Delivery SystemBoston Scientific CorporationK201159WallFlex Colonic Stent System with Anchor Lock Delivery SystemBoston Scientific CorporationK200257WallFlex Colonic Soft Stent System with Anchor Lock Delivery System, WallFlex Duodenal Soft Stent System with Anchor Lock Delivery SystemBoston Scientific CorporationK190141HANAROSTENT LowAx Colon/Rectum (NNN)M.I.Tech Co., Ltd.K183616HANAROSTENT LowAx Colon/Rectum (NNN), HANAROSTENT LowAx Duodenum/Pylorus (NNN)M.I.Tech Co., Ltd.K180180HANAROSTENT LowAxTM Colon/Rectum (NNN), HANAROSTENT LowAxTM Duodenum/Pylorus (NNN)M.I.Tech 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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