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FDA 510(k)

ARGYLE MEDIASTINAL DRAIN

K-Number: K822318 · 1982-08-27

ApplicantSherwood Medical Co.
Decision Date1982-08-27
Product CodeGBS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARGYLE MEDIASTINAL DRAIN 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 1982-08-27 under 510(k) number K822318. The device is classified under product code GBS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE MEDIASTINAL DRAIN?

ARGYLE MEDIASTINAL DRAIN is a medical device that received FDA 510(k) clearance on 1982-08-27. The listed applicant is Sherwood Medical Co.. The 510(k) number is K822318.

When did ARGYLE MEDIASTINAL DRAIN receive FDA 510(k) clearance?

ARGYLE MEDIASTINAL DRAIN received FDA 510(k) clearance on 1982-08-27, under 510(k) number K822318.

Who is the listed applicant for ARGYLE MEDIASTINAL DRAIN?

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 MEDIASTINAL DRAIN?

The FDA product code for ARGYLE MEDIASTINAL DRAIN is GBS.

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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: GBS)

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.

K912645ATRIUMS PDR THORACIC CATHETERAtrium Medical Corp.K883887AXIOM ATRAUM WOUND DRAINSAxiom, Inc.K881873INTRODUCTION/DRAINAGE CATHETER & ACCESSSheridan Catheter Corp.K880895URESIL WOUND DRAIN TROCARUresil Corp.K880376NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAPGenesis Industries, Inc.K873377CLOSED CHEST DRAINAGE SET W/SUTURESGish Biomedical, 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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