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FDA 510(k)

ARGYLE DUAL STAGE VENOUS RETURN CATH.

K-Number: K831332 · 1983-06-30

ApplicantSherwood Medical Co.
Decision Date1983-06-30
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARGYLE DUAL STAGE VENOUS RETURN CATH. is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1983-06-30 under 510(k) number K831332. 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 ARGYLE DUAL STAGE VENOUS RETURN CATH.?

ARGYLE DUAL STAGE VENOUS RETURN CATH. is a medical device that received FDA 510(k) clearance on 1983-06-30. The listed applicant is Sherwood Medical Co.. The 510(k) number is K831332.

When did ARGYLE DUAL STAGE VENOUS RETURN CATH. receive FDA 510(k) clearance?

ARGYLE DUAL STAGE VENOUS RETURN CATH. received FDA 510(k) clearance on 1983-06-30, under 510(k) number K831332.

Who is the listed applicant for ARGYLE DUAL STAGE VENOUS RETURN CATH.?

The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARGYLE DUAL STAGE VENOUS RETURN CATH.?

The FDA product code for ARGYLE DUAL STAGE VENOUS RETURN CATH. is DWF.

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Other records listing Sherwood Medical Co. as applicant

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.

K981365MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONSK960982MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULAK962880SENSI-TOUCH COMBO SPINAL/EPIDURAL REGIONAL ANESTHESIA DELIVERY SYSTEMK960574ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEMK960677KANGAROO JEJUNAL FEEDING SYSTEMK960632KANGAROO FEEDING TUBE PLACMENT STYLET

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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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