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FDA 510(k)

CATHETER, INTRAVASCULAR (ARGYLE IV SK)

K-Number: K760760 · 1976-12-09

ApplicantSherwood Medical Industries
Decision Date1976-12-09
Product CodeJCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CATHETER, INTRAVASCULAR (ARGYLE IV SK) 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 1976-12-09 under 510(k) number K760760. The device is classified under product code JCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER, INTRAVASCULAR (ARGYLE IV SK)?

CATHETER, INTRAVASCULAR (ARGYLE IV SK) is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Sherwood Medical Industries. The 510(k) number is K760760.

When did CATHETER, INTRAVASCULAR (ARGYLE IV SK) receive FDA 510(k) clearance?

CATHETER, INTRAVASCULAR (ARGYLE IV SK) received FDA 510(k) clearance on 1976-12-09, under 510(k) number K760760.

Who is the listed applicant for CATHETER, INTRAVASCULAR (ARGYLE IV SK)?

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, INTRAVASCULAR (ARGYLE IV SK)?

The FDA product code for CATHETER, INTRAVASCULAR (ARGYLE IV SK) is JCY.

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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: JCY)

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.

K863982VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAYVas-Cath of Canada , Ltd.K840324SILICONE SUMP DRAIN 20 & 40 FRENCHSuperior Plastic Products Corp.K834615TRIPLE LUMEN INFUSIONCATHETERS-Medical Components, Inc.K831453SILCATH CENTRAL CATHETER TRAY W/18 GAArgon Medical Corp.K831451SILCATH CENTRAL CATHETER TRAY SIZE-Argon Medical Corp.K822096CHEMOTHERAPY INFUSION CATHETERAmerican Heyer Schulte

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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