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FDA 510(k)

SARNS 8.0 SOFT ARC CANNULA

K-Number: K834134 · 1984-04-17

Applicant3M Health Care, Sarns
Decision Date1984-04-17
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SARNS 8.0 SOFT ARC 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 1984-04-17 under 510(k) number K834134. 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 8.0 SOFT ARC CANNULA?

SARNS 8.0 SOFT ARC CANNULA is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is 3M Health Care, Sarns. The 510(k) number is K834134.

When did SARNS 8.0 SOFT ARC CANNULA receive FDA 510(k) clearance?

SARNS 8.0 SOFT ARC CANNULA received FDA 510(k) clearance on 1984-04-17, under 510(k) number K834134.

Who is the listed applicant for SARNS 8.0 SOFT ARC 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 SARNS 8.0 SOFT ARC CANNULA?

The FDA product code for SARNS 8.0 SOFT ARC CANNULA is DWF.

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Other records listing 3M Health Care, Sarns as applicant

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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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