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FDA 510(k)

ARGYLE POLYURETHANE SALEM SUMP TUBE

K-Number: K910479 · 1991-04-19

ApplicantSherwood Medical Co.
Decision Date1991-04-19
Product CodeBSS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ARGYLE POLYURETHANE SALEM SUMP TUBE 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 1991-04-19 under 510(k) number K910479. The device is classified under product code BSS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE POLYURETHANE SALEM SUMP TUBE?

ARGYLE POLYURETHANE SALEM SUMP TUBE is a medical device that received FDA 510(k) clearance on 1991-04-19. The listed applicant is Sherwood Medical Co.. The 510(k) number is K910479.

When did ARGYLE POLYURETHANE SALEM SUMP TUBE receive FDA 510(k) clearance?

ARGYLE POLYURETHANE SALEM SUMP TUBE received FDA 510(k) clearance on 1991-04-19, under 510(k) number K910479.

Who is the listed applicant for ARGYLE POLYURETHANE SALEM SUMP TUBE?

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 POLYURETHANE SALEM SUMP TUBE?

The FDA product code for ARGYLE POLYURETHANE SALEM SUMP TUBE is BSS.

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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: BSS)

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.

K051480ENTERAL FEEDING TUBEBiosearch Medical Products, Inc.K984629MOSS TUBES, INC. NASAL TUBE - MARK IVMoss Tubes, Inc.K961711ASPISAFE GASTRIC TUBEB.Braun Medical, Inc.K933596GASTRIC, CATHETER, IRRIGATION & ASPIRATIONPolamedco, Inc.K930510RADIUS ENTERAL FEEDING TUBERadius Intl., Inc.K935688AN-10S ANDERSEN TUBE WITH STYLETH.W. Andersen Products, 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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