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FDA 510(k)

CATHETER, ARGYLE THORACIC

K-Number: K760351 · 1976-08-23

ApplicantSherwood Medical Industries
Decision Date1976-08-23
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CATHETER, ARGYLE THORACIC is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1976-08-23 under 510(k) number K760351. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER, ARGYLE THORACIC?

CATHETER, ARGYLE THORACIC is a medical device that received FDA 510(k) clearance on 1976-08-23. The listed applicant is Sherwood Medical Industries. The 510(k) number is K760351.

When did CATHETER, ARGYLE THORACIC receive FDA 510(k) clearance?

CATHETER, ARGYLE THORACIC received FDA 510(k) clearance on 1976-08-23, under 510(k) number K760351.

Who is the listed applicant for CATHETER, ARGYLE THORACIC?

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

What is the FDA product code for CATHETER, ARGYLE THORACIC?

The FDA product code for CATHETER, ARGYLE THORACIC is DWS.

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Other records listing Sherwood Medical Industries 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.

K801070SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLESK801071LANCER GLUCOSE RATE REAGENT KITK792014LANCER L-INA BUFFER, POLYMER, WASH SOLUK792013LANCER L-INA HUMAN REFERENCE SERUMK782077LANCER ICE CUBEK790523ARGYLE ESOPHAGEAL STETHOSCOPE

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Related Devices (Code: DWS)

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.

K022238MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626Medtronic VascularK964445OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006)Dlp, Inc.K962771BURKE CONGENITAL THORACOSCOPY INSTRUMENTSPilling Weck, Inc.K955689RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAYContour Fabricators of Florida, Inc.K960139G.E. STERILE ANGIOGRAPHIC TRAYGE Medical SystemsK960144G.E. STERILE CT BIOPSY TRAYGE Medical Systems

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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