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FDA 510(k)

ARGYLE GERZOF ABCESS DRAINAGE CATHETER

K-Number: K821732 · 1982-07-09

ApplicantSherwood Medical Co.
Decision Date1982-07-09
Product Code
DecisionSubstantially Equivalent

Device Summary

ARGYLE GERZOF ABCESS DRAINAGE CATHETER 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 1982-07-09 under 510(k) number K821732. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE GERZOF ABCESS DRAINAGE CATHETER?

ARGYLE GERZOF ABCESS DRAINAGE CATHETER is a medical device that received FDA 510(k) clearance on 1982-07-09. The listed applicant is Sherwood Medical Co.. The 510(k) number is K821732.

When did ARGYLE GERZOF ABCESS DRAINAGE CATHETER receive FDA 510(k) clearance?

ARGYLE GERZOF ABCESS DRAINAGE CATHETER received FDA 510(k) clearance on 1982-07-09, under 510(k) number K821732.

Who is the listed applicant for ARGYLE GERZOF ABCESS DRAINAGE CATHETER?

The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.

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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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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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