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FDA 510(k)

EQUISTREAM LONG-TERM HEMODIALYSIS CATHETERS

K-Number: K090101 · 2009-02-10

ApplicantC.R. Bard, Inc.
Decision Date2009-02-10
Product CodeMSD
Advisory CommitteeGU
DecisionUnknown

Device Summary

EQUISTREAM LONG-TERM HEMODIALYSIS CATHETERS 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 2009-02-10 under 510(k) number K090101. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the EQUISTREAM LONG-TERM HEMODIALYSIS CATHETERS?

EQUISTREAM LONG-TERM HEMODIALYSIS CATHETERS is a medical device that received FDA 510(k) clearance on 2009-02-10. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K090101.

When did EQUISTREAM LONG-TERM HEMODIALYSIS CATHETERS receive FDA 510(k) clearance?

EQUISTREAM LONG-TERM HEMODIALYSIS CATHETERS received FDA 510(k) clearance on 2009-02-10, under 510(k) number K090101.

Who is the listed applicant for EQUISTREAM LONG-TERM HEMODIALYSIS CATHETERS?

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 EQUISTREAM LONG-TERM HEMODIALYSIS CATHETERS?

The FDA product code for EQUISTREAM LONG-TERM HEMODIALYSIS CATHETERS is MSD.

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Related Devices (Code: MSD)

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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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