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FDA 510(k)

MODIFICATION OF SARNS TWO STAGE VENOUS CANNULA

K-Number: K920902 · 1993-05-11

Applicant3M Health Care, Sarns
Decision Date1993-05-11
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION OF SARNS TWO STAGE VENOUS CANNULA 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 1993-05-11 under 510(k) number K920902. 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 MODIFICATION OF SARNS TWO STAGE VENOUS CANNULA?

MODIFICATION OF SARNS TWO STAGE VENOUS CANNULA is a medical device that received FDA 510(k) clearance on 1993-05-11. The listed applicant is 3M Health Care, Sarns. The 510(k) number is K920902.

When did MODIFICATION OF SARNS TWO STAGE VENOUS CANNULA receive FDA 510(k) clearance?

MODIFICATION OF SARNS TWO STAGE VENOUS CANNULA received FDA 510(k) clearance on 1993-05-11, under 510(k) number K920902.

Who is the listed applicant for MODIFICATION OF SARNS TWO STAGE VENOUS CANNULA?

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 MODIFICATION OF SARNS TWO STAGE VENOUS CANNULA?

The FDA product code for MODIFICATION OF SARNS TWO STAGE VENOUS CANNULA is DWF.

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Other records listing 3M Health Care, Sarns as applicant

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K960916SAMS 8000 CARDIOPLEGIA MONITORK953901SARNS 800 ROLLER PUMPK9507393M SARNS FLOW SENSOR, CENTRIFUGAL CONTROL MODULE 115, 220 V, 900 PERFUSION SYSTEMK941653SARNS TURBO MEMBRANE OXYGENATOR MODIFICATIONK941654SARNS FILTERED VENOUS RESERVIOR MODIFICATIONK940651SARNS ULTRASONIC AIR SENSOR

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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.

K260195Elongated One-Piece Arterial (EOPA) 3D™ Arterial CannulaeMedtronic, Inc.K250937Venous Return CannulaeLivaNova USA, Inc.K260043Smart Reactors Camouflage Coated Extracorporeal Cardiopulmonary Tubing Set (SR180C)Smart ReactorsK253203Retrograde Coronary Sinus Perfusion CannulaeMedtronic, Inc.K253671Dual Stage Venous CannulaeSorin Group Italia S.R.L.K253998Clearview Intracoronary ShuntsMedtronic, Inc.

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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