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FDA 510(k)

CATHETER CONNECTOR, ARGYLE TUBING

K-Number: K760524 · 1976-11-02

ApplicantSherwood Medical Industries
Decision Date1976-11-02
Product CodeGCD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CATHETER CONNECTOR, ARGYLE TUBING 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 1976-11-02 under 510(k) number K760524. The device is classified under product code GCD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER CONNECTOR, ARGYLE TUBING?

CATHETER CONNECTOR, ARGYLE TUBING is a medical device that received FDA 510(k) clearance on 1976-11-02. The listed applicant is Sherwood Medical Industries. The 510(k) number is K760524.

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

CATHETER CONNECTOR, ARGYLE TUBING received FDA 510(k) clearance on 1976-11-02, under 510(k) number K760524.

Who is the listed applicant for CATHETER CONNECTOR, ARGYLE TUBING?

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 CONNECTOR, ARGYLE TUBING?

The FDA product code for CATHETER CONNECTOR, ARGYLE TUBING is GCD.

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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: GCD)

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.

K952470ACTI-FLEX LOW, MEDIUM, RESCARE I, RESCARE II.R-Group Intl.K940198L-CATH CONNECTOR ASSEMBLYLuther Medical Products, Inc.K863446ANGIOMED HIGH PRESSURE CONNECTORSAngiomed U.S., Inc.K851196INCISION DRAINSil-Med Corp.K851921Y CONNECTORSil-Med Corp.K760382CONNECTORSB. Braun Instruments

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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