FDA 510(k)

SARNS WIRE-REINFORCED VENOUS RETURN CAN

K-Number: K790246 · 1979-03-02

Decision Date1979-03-02

Product CodeDWF

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

SARNS WIRE-REINFORCED VENOUS RETURN CAN 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 1979-03-02 under 510(k) number K790246. 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 SARNS WIRE-REINFORCED VENOUS RETURN CAN?

SARNS WIRE-REINFORCED VENOUS RETURN CAN is a medical device that received FDA 510(k) clearance on 1979-03-02. The listed applicant is 3M Health Care, Sarns. The 510(k) number is K790246.

When did SARNS WIRE-REINFORCED VENOUS RETURN CAN receive FDA 510(k) clearance?

SARNS WIRE-REINFORCED VENOUS RETURN CAN received FDA 510(k) clearance on 1979-03-02, under 510(k) number K790246.

Who is the listed applicant for SARNS WIRE-REINFORCED VENOUS RETURN CAN?

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 SARNS WIRE-REINFORCED VENOUS RETURN CAN?

The FDA product code for SARNS WIRE-REINFORCED VENOUS RETURN CAN is DWF.

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Other records listing 3M Health Care, Sarns as applicant

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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.