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FDA 510(k)

MEDSURG 7 FR. DUAL LUMEN CENTRAL VEIN CATH SYSTEM

K-Number: K880771 · 1988-05-03

ApplicantMedsurg Industries, Inc.
Decision Date1988-05-03
Product CodeDQR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDSURG 7 FR. DUAL LUMEN CENTRAL VEIN CATH SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medsurg Industries, Inc.. It received FDA 510(k) clearance on 1988-05-03 under 510(k) number K880771. The device is classified under product code DQR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDSURG 7 FR. DUAL LUMEN CENTRAL VEIN CATH SYSTEM?

MEDSURG 7 FR. DUAL LUMEN CENTRAL VEIN CATH SYSTEM is a medical device that received FDA 510(k) clearance on 1988-05-03. The listed applicant is Medsurg Industries, Inc.. The 510(k) number is K880771.

When did MEDSURG 7 FR. DUAL LUMEN CENTRAL VEIN CATH SYSTEM receive FDA 510(k) clearance?

MEDSURG 7 FR. DUAL LUMEN CENTRAL VEIN CATH SYSTEM received FDA 510(k) clearance on 1988-05-03, under 510(k) number K880771.

Who is the listed applicant for MEDSURG 7 FR. DUAL LUMEN CENTRAL VEIN CATH SYSTEM?

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

What is the FDA product code for MEDSURG 7 FR. DUAL LUMEN CENTRAL VEIN CATH SYSTEM?

The FDA product code for MEDSURG 7 FR. DUAL LUMEN CENTRAL VEIN CATH SYSTEM is DQR.

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Other records listing Medsurg Industries, Inc. as applicant

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K920780MEDSURG INSERTION TRAYK940175MEDSURG STERILE O.R. TOWELSK934731MEDSURG STERILE IMAGING PRODUCTSK925558INFILTUBEK934971STERILE LAPAROTOMY SPONGESK920421MEDSURG MARSHMALLOW TRAY

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Related Devices (Code: DQR)

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.

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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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