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FDA 510(k)

CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL.

K-Number: K880103 · 1988-03-22

ApplicantResearch Medical, Inc.
Decision Date1988-03-22
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL. is the device name listed in this FDA 510(k) record. The listed applicant is Research Medical, Inc.. It received FDA 510(k) clearance on 1988-03-22 under 510(k) number K880103. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL.?

CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL. is a medical device that received FDA 510(k) clearance on 1988-03-22. The listed applicant is Research Medical, Inc.. The 510(k) number is K880103.

When did CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL. receive FDA 510(k) clearance?

CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL. received FDA 510(k) clearance on 1988-03-22, under 510(k) number K880103.

Who is the listed applicant for CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL.?

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

What is the FDA product code for CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL.?

The FDA product code for CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL. is DWF.

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Related Devices (Code: DWF)

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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