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FDA 510(k)

ARGYLE PEDIATRIC URINE COLLECTOR

K-Number: K813479 · 1982-01-07

ApplicantSherwood Medical Co.
Decision Date1982-01-07
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ARGYLE PEDIATRIC URINE COLLECTOR 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 1982-01-07 under 510(k) number K813479. The device is classified under product code KNX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE PEDIATRIC URINE COLLECTOR?

ARGYLE PEDIATRIC URINE COLLECTOR is a medical device that received FDA 510(k) clearance on 1982-01-07. The listed applicant is Sherwood Medical Co.. The 510(k) number is K813479.

When did ARGYLE PEDIATRIC URINE COLLECTOR receive FDA 510(k) clearance?

ARGYLE PEDIATRIC URINE COLLECTOR received FDA 510(k) clearance on 1982-01-07, under 510(k) number K813479.

Who is the listed applicant for ARGYLE PEDIATRIC URINE COLLECTOR?

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 PEDIATRIC URINE COLLECTOR?

The FDA product code for ARGYLE PEDIATRIC URINE COLLECTOR is KNX.

Related Clinical Trials

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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: KNX)

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.

K110518IBAGFuture Path Medical, LLCK9733644L DRAINAGE BAG, 4L BAG FOR PERITONEAL DIALYSIS, 4L URINARY DRAINAGE BAGMaersk Medical A/SK972887MEDLINE PREMIUM LEG BAG, MEDLINE FABRIC BAC LEG BAG, MEDLINE URINARY LEG BAGMedline Industries, Inc.K971271BESECURE EXTERNAL URINARY COLLECTION SYSTEMUrology Research Intl., Inc.K971929AMSINO URINARY LEG BAGAmsino Intl., Inc.K971764WELCON HUE-VU URINARY DRAINAGE BAGWelcon, 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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