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FDA 510(k)

ARGYLE ENTERITE ENTERAL FEEDING PUMP

K-Number: K842421 · 1984-08-17

ApplicantSherwood Medical Co.
Decision Date1984-08-17
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ARGYLE ENTERITE ENTERAL FEEDING PUMP 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 1984-08-17 under 510(k) number K842421. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE ENTERITE ENTERAL FEEDING PUMP?

ARGYLE ENTERITE ENTERAL FEEDING PUMP is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Sherwood Medical Co.. The 510(k) number is K842421.

When did ARGYLE ENTERITE ENTERAL FEEDING PUMP receive FDA 510(k) clearance?

ARGYLE ENTERITE ENTERAL FEEDING PUMP received FDA 510(k) clearance on 1984-08-17, under 510(k) number K842421.

Who is the listed applicant for ARGYLE ENTERITE ENTERAL FEEDING PUMP?

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 ENTERITE ENTERAL FEEDING PUMP?

The FDA product code for ARGYLE ENTERITE ENTERAL FEEDING PUMP is FRN.

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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: FRN)

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.

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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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