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FDA 510(k)

ARGYLE SUCTION CONTROL KIT

K-Number: K760601 · 1976-11-01

ApplicantSherwood Medical Co.
Decision Date1976-11-01
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARGYLE SUCTION CONTROL KIT 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 1976-11-01 under 510(k) number K760601. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE SUCTION CONTROL KIT?

ARGYLE SUCTION CONTROL KIT is a medical device that received FDA 510(k) clearance on 1976-11-01. The listed applicant is Sherwood Medical Co.. The 510(k) number is K760601.

When did ARGYLE SUCTION CONTROL KIT receive FDA 510(k) clearance?

ARGYLE SUCTION CONTROL KIT received FDA 510(k) clearance on 1976-11-01, under 510(k) number K760601.

Who is the listed applicant for ARGYLE SUCTION CONTROL KIT?

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 SUCTION CONTROL KIT?

The FDA product code for ARGYLE SUCTION CONTROL KIT is GCY.

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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: GCY)

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.

K972703REDYROB-CLOSED WOUND DRAINAGE SYSTEMB.Braun Medical, Inc.K971036ODONTIT AUTOGENOUS BONE COLLECTION DEVICEInterpore Intl.K963839CORDIS SUCTION RESERVOIR - MODEL NUMBER: 910-500Cordis Corp.K960099PENROSE DRAIN MODELS 6001 - 6007Sil-Med Corp.K950754MACRO SUCTION TUBE MODEL NO 10061Dlp, Inc.K936223PRESSURE IRRIGATING SYSTEMLevel 1 Technologies, 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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