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FDA 510(k)

ARGYLE RIGID URINE MEASURING/COLL. DEV.

K-Number: K801522 · 1980-07-28

ApplicantSherwood Medical Co.
Decision Date1980-07-28
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ARGYLE RIGID URINE MEASURING/COLL. DEV. 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 1980-07-28 under 510(k) number K801522. 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 RIGID URINE MEASURING/COLL. DEV.?

ARGYLE RIGID URINE MEASURING/COLL. DEV. is a medical device that received FDA 510(k) clearance on 1980-07-28. The listed applicant is Sherwood Medical Co.. The 510(k) number is K801522.

When did ARGYLE RIGID URINE MEASURING/COLL. DEV. receive FDA 510(k) clearance?

ARGYLE RIGID URINE MEASURING/COLL. DEV. received FDA 510(k) clearance on 1980-07-28, under 510(k) number K801522.

Who is the listed applicant for ARGYLE RIGID URINE MEASURING/COLL. DEV.?

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 RIGID URINE MEASURING/COLL. DEV.?

The FDA product code for ARGYLE RIGID URINE MEASURING/COLL. DEV. 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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