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FDA 510(k)

VASCATH OPTI-FLOW LONG TERM DUAL LUMEN HEMODIALYSIS CATHETER

K-Number: K981994 · 1998-09-03

ApplicantC.R. Bard, Inc.
Decision Date1998-09-03
Product CodeMSD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VASCATH OPTI-FLOW LONG TERM DUAL LUMEN HEMODIALYSIS CATHETER 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 1998-09-03 under 510(k) number K981994. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASCATH OPTI-FLOW LONG TERM DUAL LUMEN HEMODIALYSIS CATHETER?

VASCATH OPTI-FLOW LONG TERM DUAL LUMEN HEMODIALYSIS CATHETER is a medical device that received FDA 510(k) clearance on 1998-09-03. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K981994.

When did VASCATH OPTI-FLOW LONG TERM DUAL LUMEN HEMODIALYSIS CATHETER receive FDA 510(k) clearance?

VASCATH OPTI-FLOW LONG TERM DUAL LUMEN HEMODIALYSIS CATHETER received FDA 510(k) clearance on 1998-09-03, under 510(k) number K981994.

Who is the listed applicant for VASCATH OPTI-FLOW LONG TERM DUAL LUMEN HEMODIALYSIS CATHETER?

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 VASCATH OPTI-FLOW LONG TERM DUAL LUMEN HEMODIALYSIS CATHETER?

The FDA product code for VASCATH OPTI-FLOW LONG TERM DUAL LUMEN HEMODIALYSIS CATHETER 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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