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FDA 510(k)

FLOWGUARD CATHETERS & CANNALAE

K-Number: K813037 · 1981-12-14

ApplicantAdvocacy International, Ltd.
Decision Date1981-12-14
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FLOWGUARD CATHETERS & CANNALAE is the device name listed in this FDA 510(k) record. The listed applicant is Advocacy International, Ltd.. It received FDA 510(k) clearance on 1981-12-14 under 510(k) number K813037. 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 FLOWGUARD CATHETERS & CANNALAE?

FLOWGUARD CATHETERS & CANNALAE is a medical device that received FDA 510(k) clearance on 1981-12-14. The listed applicant is Advocacy International, Ltd.. The 510(k) number is K813037.

When did FLOWGUARD CATHETERS & CANNALAE receive FDA 510(k) clearance?

FLOWGUARD CATHETERS & CANNALAE received FDA 510(k) clearance on 1981-12-14, under 510(k) number K813037.

Who is the listed applicant for FLOWGUARD CATHETERS & CANNALAE?

The FDA 510(k) record lists Advocacy International, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLOWGUARD CATHETERS & CANNALAE?

The FDA product code for FLOWGUARD CATHETERS & CANNALAE is DWF.

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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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