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FDA 510(k)

ARGYLE SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAY

K-Number: K935781 · 1995-01-27

ApplicantSherwood Medical Co.
Decision Date1995-01-27
Product CodeFEG
Advisory CommitteeGU
DecisionUnknown

Device Summary

ARGYLE SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAY 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 1995-01-27 under 510(k) number K935781. The device is classified under product code FEG. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ARGYLE SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAY?

ARGYLE SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAY is a medical device that received FDA 510(k) clearance on 1995-01-27. The listed applicant is Sherwood Medical Co.. The 510(k) number is K935781.

When did ARGYLE SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAY receive FDA 510(k) clearance?

ARGYLE SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAY received FDA 510(k) clearance on 1995-01-27, under 510(k) number K935781.

Who is the listed applicant for ARGYLE SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAY?

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 SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAY?

The FDA product code for ARGYLE SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAY is FEG.

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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: FEG)

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.

K17161914Fr Colon Decompression Set, Macon Colon Decompression SetCook Ireland, Ltd.K132314MEDLINE ANTI-REFLUX VALVEMedline Industries, Inc.K053410GIENTRIPORT WITH UNIVERSAL SINGLE LUMEN ADAPTORKendallK040388NEXT GENERATION SALEM SUMPKendallK971354KNOTT NG TUBEMichael M. Knott, M.D.K960176DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTERC.R. Bard, 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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