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FDA 510(k)

ARGYLE A-V MEDI-WING HEMODIALYSIS SET

K-Number: K801618 · 1980-08-13

ApplicantSherwood Medical Co.
Decision Date1980-08-13
Product CodeFIE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ARGYLE A-V MEDI-WING HEMODIALYSIS SET 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 1980-08-13 under 510(k) number K801618. The device is classified under product code FIE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE A-V MEDI-WING HEMODIALYSIS SET?

ARGYLE A-V MEDI-WING HEMODIALYSIS SET is a medical device that received FDA 510(k) clearance on 1980-08-13. The listed applicant is Sherwood Medical Co.. The 510(k) number is K801618.

When did ARGYLE A-V MEDI-WING HEMODIALYSIS SET receive FDA 510(k) clearance?

ARGYLE A-V MEDI-WING HEMODIALYSIS SET received FDA 510(k) clearance on 1980-08-13, under 510(k) number K801618.

Who is the listed applicant for ARGYLE A-V MEDI-WING HEMODIALYSIS SET?

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 A-V MEDI-WING HEMODIALYSIS SET?

The FDA product code for ARGYLE A-V MEDI-WING HEMODIALYSIS SET is FIE.

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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.

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Related Devices (Code: FIE)

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.

K253469Ritus™ Safety Fistula Cannula with Anti-Reflux Valve 15G x 30mm (1530VSMM); Ritus™ Safety Fistula Cannula with Anti-Reflux Valve 15G x 38mm (1538VSMM); Ritus™ Safety Fistula Cannula with Anti-Reflux Valve 16G x 30mm (1630VSMM); Ritus™ Safety Fistula Cannula with Anti-Reflux Valve 16G x 38mm (1638VSMM); Ritus™ Safety Fistula Cannula with Anti-Reflux Valve 17G x 30mm (1730VSMM); Ritus™ Safety Fistula Cannula with Anti-Reflux Valve 17G x 38mm (1738VSMM)Mozarc Medical Us, LLCK251877JMS CAVEO A.V. Fistula Needle SetJMS North America CorporationK213015DORA Disposable A.V. Fistula Needle SetsBain Medical Equipment (Guangzhou) Co., Ltd.K171505Dimesol Disposable AV Fistula Needle Set (Non-Safety Series) and Dimesol Disposable AV Fistula Needle Set (Safety Series)Dimesol, Inc.K163025DORA Disposable A.V. Fistula Needle SetsBain Medical Equipment (Guangzhou) Co., Ltd.K112734APLAN A.V. FISTULA NEEDLE SETAplan Well Enterprise Co., Ltd.

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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