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FDA 510(k)

CATHETER, TWO STAGE VENOUS RETURN

K-Number: K770431 · 1977-03-16

Applicant3M Health Care, Sarns
Decision Date1977-03-16
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CATHETER, TWO STAGE VENOUS RETURN is the device name listed in this FDA 510(k) record. The listed applicant is 3M Health Care, Sarns. It received FDA 510(k) clearance on 1977-03-16 under 510(k) number K770431. 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, TWO STAGE VENOUS RETURN?

CATHETER, TWO STAGE VENOUS RETURN is a medical device that received FDA 510(k) clearance on 1977-03-16. The listed applicant is 3M Health Care, Sarns. The 510(k) number is K770431.

When did CATHETER, TWO STAGE VENOUS RETURN receive FDA 510(k) clearance?

CATHETER, TWO STAGE VENOUS RETURN received FDA 510(k) clearance on 1977-03-16, under 510(k) number K770431.

Who is the listed applicant for CATHETER, TWO STAGE VENOUS RETURN?

The FDA 510(k) record lists 3M Health Care, Sarns as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CATHETER, TWO STAGE VENOUS RETURN?

The FDA product code for CATHETER, TWO STAGE VENOUS RETURN is DWF.

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Related Devices (Code: 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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