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FDA 510(k)

CATHETER, UMBILICAL ARTERY

K-Number: K760966 · 1977-01-26

ApplicantSherwood Medical Industries
Decision Date1977-01-26
Product CodeFOS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CATHETER, UMBILICAL ARTERY 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 1977-01-26 under 510(k) number K760966. The device is classified under product code FOS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER, UMBILICAL ARTERY?

CATHETER, UMBILICAL ARTERY is a medical device that received FDA 510(k) clearance on 1977-01-26. The listed applicant is Sherwood Medical Industries. The 510(k) number is K760966.

When did CATHETER, UMBILICAL ARTERY receive FDA 510(k) clearance?

CATHETER, UMBILICAL ARTERY received FDA 510(k) clearance on 1977-01-26, under 510(k) number K760966.

Who is the listed applicant for CATHETER, UMBILICAL ARTERY?

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, UMBILICAL ARTERY?

The FDA product code for CATHETER, UMBILICAL ARTERY is FOS.

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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: FOS)

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.

K201697Umbilical Vessels CatheterHaolang Medical USA CorporationK130725MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.Covidien Lp, Formerly Registered AS KendallK120304FOOTPRINT MEDICAL POLYURETHANE UMBILICAL CATHETERFootprint Medical, Inc.K091214FOOTPRINT MEDICAL SILICONE UMBILICAL CATHETERFootprint MedicalK091213FOOTPRINT MEDICAL UMBILICAL CATHETER, DUAL LUMENFootprint MedicalK081515NEOMED DUAL LUMEN UMBILICAL CATHETER, MODELS S2UVC4.0, S2UVC5.0Neomed, 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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